2024-03-28T21:28:58Z
https://www.pacificejournals.com/journal/index.php/aabs/oai
oai:ojs.localhost:article/305
2015-06-26T17:47:40Z
aabs:CR
ITP- Immune Thrombocytopenia: A Case Report
Jaison, Janice
Joshi, Ramdas
Joshi, Sneha Ramdas
Until recently, the abbreviation ITP stood for idiopathic thrombocytopenic purpura, but current awareness relating to the immune-mediated nature of the disease, and the absence or minimal signs of bleeding in a large proportion of cases have led to a revision of the terminology. We present a case of Primary immune thrombocytopenia. This article also provides an update on the current definitions related to immune thrombocytopenia, as per recommendations of an International Working Group (IWG) on ITP.
Pacific Group of e-Journals (PaGe)
2015-04-06
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/305
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C1-C5
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/305/pdf_20
oai:ojs.localhost:article/327
2015-06-26T17:47:40Z
aabs:CR
Anaplastic Thyroid carcinoma: A Rare Case
Nagare, Mangala Rajesh
Joshi, Sneha Ramdas
Karwande, Ashwini Vishal
Pathak, Smita Shripad
Tekwani, Deepa Topandas
Jaison, Janice
Abstract -Anaplastic carcinoma of thyroid is one of the most lethal tumours in humans. They are rare and usually occur in cases of long standing thyroid disease and other thyroid tumours. Prognosis is poor with a mean survival rate of about 6 months after diagnosis. However patients with small foci of anaplastic carcinoma, in well-differentiated thyroid tumours, that are excised completely, are reported to have better survival rates. Death is usually due to local recurrence or distant metastasis to lungs, bone or brain.We report an interesting case of anaplastic thyroid carcinoma, in a 47 year old lady with longstanding co-existing goiter.
Pacific Group of e-Journals (PaGe)
2015-04-29
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/327
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C6-C9
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/327/pdf_23
oai:ojs.localhost:article/345
2015-06-26T17:47:40Z
aabs:CR
Persistent mullerian duct syndrome: A case report
Godbole, Chandrahas Ramesh
Joshi, Sneha
Jaison, Janice
Persistent mullerian duct syndrome (PMDS) is usually an accidental finding either during orchipexy or during routine inguinal hernia repair in male patients presenting with maldescended or cryptorchid testes. It is caused by a defect in the mullerian inhibiting factor. Intraoperatively, mullerian remnants consisting of an infantile uterus and fallopian tubes are usually found. Familiarity with PMDS is necessary to diagnose the condition. We report a case of PMDS in a 45-year-old male presenting with right inguinal hernia.
Pacific Group of e-Journals (PaGe)
2015-05-26
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/345
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C10-C13
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/345/pdf_25
oai:ojs.localhost:article/364
2015-06-26T17:47:40Z
aabs:CR
Isolated cysticercus cellulosae of medial rectus muscle presenting with a mass over the inner region of the eye – a rare case report and treatment review
Rana, Jagriti
Singh, S P
Jha, Vijay Kumar
Khanduja, S
Ocular involvement with or without brain involvement is common in Cysticercosis but isolated Cysticercus cellulosae of medial rectus muscle is very rare. Herein we are presenting a case of isolated cysticercosis of medial rectus in young male which was diagnosed on radiology and responded well to albendazole and predinisolone.
Pacific Group of e-Journals (PaGe)
2015-06-05
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/364
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C14-C17
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/364/pdf_26
oai:ojs.localhost:article/367
2015-06-26T17:47:40Z
aabs:CR
Acute Eosinophilic Appendicitis: Case report of three cases with brief review of literature
Kumbar, Rajeshwari Karibasappa
Dravid, N V
GN, Karibasappa
Surana, Akshay
Acute eosinophilic appendicitis (AEA) is a rare variant of appendix inflammation. The histologic hallmark of this entity is eosinophilic infiltration of the musularis layer with accompanying oedema separating the muscle fibres with out neutrophilic infiltration.To the best of our knowledge there are very few cases of eosinophilic appendicitis (EA) in the absence of any other abnormality reported in the literature. Hence, we made an attempt to study the cases of AEA and to draw the relevant conclusion about the disease pathogenesis. Out of total 159 appendectomy cases, three cases were found to have eosinophilic appendicitis (EA) and these cases were studied for clinical and pathological findings. Incidence of 0.02% (3/15) with male preponderance was found. We herein, present the cases of AEA which is rare variant and less understood entity.
Pacific Group of e-Journals (PaGe)
2015-06-05
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/367
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C18-C21
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/367/pdf_27
oai:ojs.localhost:article/372
2015-06-26T17:47:40Z
aabs:CR
Hemoglobin H Disease: A rare case report and its diagnostic challenge.
Sindhu, R
Behera, S K
Mishra, D P
Thalassemia the most common monogenic gene disorder in the world is especially frequent in Mediterranean countries. Hemoglobin H (Hb H) disease is a special variant of α-thalassemia presenting as microcytic hypochromic anemia. The clinical phenotypes of most individuals remain unnoticed unless there occurs an acute hemolytic crisis and they are most often underdiagnosed or misdiagnosed as iron deficiency anemia. Here we report a case of 34 year old pregnant women who presented with pallor and mild splenomegaly. Complete blood count (CBC) showed decrease in Mean Corpuscular Volume (MCV), Mean Corpuscular Hemoglobin (MCH), Mean Corpuscular Hemoglobin Concentration (MCHC) and increase in Red Cell Distribution Width (RDW) and reticulocyte percent. Peripheral smear showed microcytic hypochromic Red Blood Corpuscles (RBCs) with severe anisopoikilocytosis. Supravital staining of peripheral blood showed Hb H inclusions in RBCs. The increase in reticulocyte percent here is due to mature RBC’s having Hb H inclusions that are misinterpreted as reticulocytes by automated cell counters. Hence, in a background of variable clinical presentation of this disease, we consider this case to highlight the importance of simple peripheral smear examination and supravital staining of peripheral blood in the diagnosis of Hb H disease which are often misdiagnosed as iron deficiency anemia by seeing CBC results. It is also important to emphasize the importance of early diagnosis of these cases to facilitate implementation of proper preventive health care measure, ensure fetal well being and prompt treatment of potentially serious hemolytic crisis that can occur during pregnancy.
Pacific Group of e-Journals (PaGe)
2015-06-16
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/372
Annals of Applied Bio-Sciences; Vol 2 No 2 (2015); C22-C24
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/372/pdf_29
oai:ojs.localhost:article/375
2015-10-19T19:44:18Z
aabs:CR
Selective IgM deficiency presenting as chronic diarrhea: A case report
Usha, .
Gupta, Ashish Kumar
Kumar, Mohan
Mishra, O P
Sinha, Amit Kumar
Primary immunodeficiency (PID) is a heterogeneous disorder resulting from reduced or absent function of one of the components of immune system like T-cells, B-cells, NK cells, neutrophils, its receptor, immunoglobulins, complements and genes responsible for rearrangement of T- cell receptor and immunoglobulin and its signaling molecule. Among the clinical manifestation sinusitis, pneumonia, bronchiectasis, allergic disease, autoimmune disease and diarrhea are common manifestation in Antibodies deficiency.A 4-years-old boy presented with chronic diarrhea and failure to grow. On endoscopy, there was nodule in D2 region which, on histopathological examination showed features mimicking as celiac disease. His serum anti-TTg Ab was within normal limits and serum Ig M was deficient.
Pacific Group of e-Journals (PaGe)
2015-06-26
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs375
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C29-31
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs375/pdf_30
oai:ojs.localhost:article/380
2015-10-19T19:44:18Z
aabs:CR
Primary Breast Lymphoma: a rare case report with emphasis on role of cytology, cell block and tru-cut biopsy in diagnosis
Chaudhuri, Arnab
Samaddar, Aparajita
Nag, Dipanwita
Introduction: Primary breast lymphoma (PBL) is a rare tumour of breast and constitutes <0.6% of all breast malignancies and 2.2% of extranodal lymphomas. More than 80% of the PBL are B-cell Lymphoma, the most frequent being diffuse large B cell lymphoma.Case History: A sixty seven year old female presented with a 5X4 cm, firm, non-tender, mobile mass in lower-inner quadrant of left breast for last one month. Mammography suggested it to be a case of fibroadenoma. FNAC from the swelling diagnosed it as a case of Non-Hodgkin’s Lymphoma (NHL), with poorly differentiated ductal carcinoma as differential diagnosis. Cell block and tru-cut biopsy corroborated the FNAC findings. Immunohistochemistry definitely proved it to be a case of Primary Breast NHL.Conclusions: PBL can present as an innocuous lump. Early diagnosis is important for better prognosis. FNAC along with cell block, tru-cut biopsy with immunochemistry can diagnose a case and unnecessary surgical intervention can be avoided. We are reporting this case because it is a rare case and to emphasize on the role of FNAC, cell-block and tru-cut biopsy in diagnosis to prevent unnecessary mastectomies.
Pacific Group of e-Journals (PaGe)
2015-06-26
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs380
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C25-28
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs380/pdf_31
oai:ojs.localhost:article/396
2015-10-19T19:44:18Z
aabs:CR
Metastasizing ameloblastoma: A case report
Godbole, Chandrahas Ramesh
Pathak, Smita
Ameloblastoma is the most common odontogenic tumor, but the incidence of its metastasis is low. We report a case of recurrent ameloblastoma metastasizing to the cervical lymph node. This patient presented with a radiolucent cystic lesion in the left mandibular region. Segmental mandibulectomy along with cervical lymph node dissection was performed. Histopathological features revealed an ameloblastoma with single lymph node metastasis. The patient had two previous instances of lesion at same site which were diagnosed to be ameloblastoma on histopathology. Metastasizing ameloblatomas are different from ameloblastic carcinomas and lymph node metastasis is especially rare. The case is presented as it exhibits this peculiar feature.
Pacific Group of e-Journals (PaGe)
2015-07-08
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs396
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C32-34
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs396/pdf_32
oai:ojs.localhost:article/404
2015-10-19T19:44:18Z
aabs:CR
Russell’s viper bite on glans penis: An unusual case study
Mallik, Subhendu
Sahoo, Sangeeta
Mohanty, Manoj Kumar
Singh, Sudipta Ranjan
Padhy, Niranjan
Snake bite is a major public health issue in tropical countries. The usual bite sites are extremities. We report a rare case where the victim was bitten by a new born Russell’s viper (Daboia russellii) on the glans penis while sleeping on the ground in night. The patient was successfully treated and discharged uneventfully. We have discussed the various aspects of the unusual bite.
Pacific Group of e-Journals (PaGe)
2015-07-13
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs404
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C35-38
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs404/pdf_33
oai:ojs.localhost:article/416
2015-10-19T19:44:18Z
aabs:CR
Ocular Rhinosporidium Granuloma masquerading as Conjunctival Hemangioma: a Case Report
Raina, Bawana
Lahori, Mega
Khajuria, Arvind
Ocular rhinosporidiosis is a chronic granulomatous infection caused by Rhinosporidium seeberi, a protistal microorganism endemic in the hot, tropical climes of India and Sri Lanka. It often presents as a friable, vascular conjunctival polyp but may mimic other ocular conditions. We present the case of a 35 year old female with an ocular polypoid mass that resembled a conjunctival hemangioma but was proved to be Ocular rhinosporidiosis on histopathology. Thick walled sporangia of Rhinosporidium seeberi containing multiple nucleated endospores are the typical diagnostic features on histopathology. Total wide-base excision of the polyp, preferably by electro-cautery, is recommended to prevent spillage of endospores and recurrence of the lesion. This is the first reported case of ocular rhinosporidiosis from Jammu & Kashmir state of North India.
Pacific Group of e-Journals (PaGe)
2015-08-04
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs416
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C39-41
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs416/pdf_37
oai:ojs.localhost:article/425
2015-10-19T19:44:18Z
aabs:CR
Sudden Death Due To Rupture Of Pseudoaneurysm : A Rare Case
Sethi, Abarnita
Jena, Manoj Kumar
Sethi, Sudhansu Sekhar
Rupture of ventricular pseudoaneurysm (PSA) as a complication of Acute myocardial infarction is a rare cause of sudden death. PSA may lead to fatality by rupture /thromboembolism, the force of myocardiac contraction leads to rupture. We discuss here a case of such sudden death which resulted out of such a rare condition. A person died within 2-3 hours of chest pain during referral without investigation and treatment. On autopsy rupture of pseudoaneurysm was detected on the posterolateral wall of left ventricle. We intend to discuss the findings of this rare case and through light upon the importance of regular treatment to avoid such complications.
Pacific Group of e-Journals (PaGe)
2015-08-16
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs425
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C42-45
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs425/pdf_38
oai:ojs.localhost:article/445
2015-10-19T19:44:18Z
aabs:CR
Congenital hepatic fibrosis in a case of Autosomal Dominant Polycystic Kidney Disease: A case report of rare association and review of literature
Gaikwad, Vaishali
Gadgil, Nitin
Majethia, Nikhil
Kalgutkar, Alka
Cilliopathies are the newer group of human genetic disorders in which the cilliary structure or function is affected. Hepatorenal fibrocystic diseases (HRFCDs) are a part of cilliopathies and characterized by developmental abnormalities of the portobiliary system along with fibrocystic change in the kidneys. Polycystic kidney diseases (PKD) which is the largest subclass of HRFCDs had autosomal dominant and recessive forms. ADPKD is characterized by multiple, bilateral renal cysts along with extra renal manifestations .Liver is the most common extra renal organ affected in ADPKD. Congenital hepatic fibrosis (CHF), is the rare but well known forms of liver involvement in ADPKD.We report a case of a 26 year male was admitted to Lokmanya Tilak Municipal Hospital for sudden loss of consciousness and one episode of convulsion.Patient succumbed to his illness within two hours, autopsy revealed bilaterally enlarged polycystic kidneys.Liver showed broad bands of portal to portal fibrosis. The portal tracts contained abundant irregularly shaped interlobular bile ducts. Congenital hepatic fibrosis (CHF) is most commonly associated with ARPKD amongst the various renal cilliopathies. We present the rare association of ADPKD with CHF.
Pacific Group of e-Journals (PaGe)
2015-08-25
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs445
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C46-49
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs445/pdf_40
oai:ojs.localhost:article/448
2015-10-19T19:44:18Z
aabs:CR
ROUND CELL VARIANT OF MYXOID LIPOSARCOMA IN A YOUNG FEMALE AT ELBOW : A CASE REPORT
Agrawal, Prahlad Chandra
Naik, Reena
Jangade, Praveen
Round cell variant of myxoid liposarcoma (MRCLS) is a type of liposarcoma though classified separately(WHO),shares common clinical& morphological features. As compare with other types, this variant has younger onset with peak at 35-55 years with male predominance. It predomintly affects limbs particularily thigh & rarely arises from retroperitoneum & subcutaneous tissue. Presence of more round cells in myxoid background (hypercellularity) pointed towards bad prognosis. We are here reporting a case of round cell variant of myxoid liposarcoma in 30 years female, diagnosed in histopathology, composed of uniform spindle cells, round cells with signet ring lipoblasts in prominent background of myxoid stroma with plexiform vasculature, which ,was negative in the cytology. CT scan shows, soft tissue density mass in the subcutaneous area of the right elbow. The presentation of our case is unique in the regard that, age,sex & the site (extensor surface of elbow), where minimal fatty tissue presents.
Pacific Group of e-Journals (PaGe)
2015-09-02
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aas448b
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C50-53
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aas448b/pdf_41
oai:ojs.localhost:article/453
2015-10-19T19:44:18Z
aabs:CR
Hereditary Ectodermal Dysplasia: A Case Report
Kumar, Virender
Kumar, Lalit
Ectodermal dysplasia (ED) is a hereditary disease characterized by anomalies in the structures of ectodermal origin. The disease affects skin, saliva, sebaceous and sweat glands (anhidrosis or hypohidrosis), hair (atrichosis or hypotrichosis), nail and teeth (anodontia or hypodontia). Oral rehabilitation is important from a functional, esthetic and psychological standpoint. A team approach, that includes input from Peadodontist, an Orthodontist, a Prosthodontist and an Oral and maxillofacial surgeon, is necessary for a successful outcome. This paper discusses a case of Hypohidrotic Ectodermal Dysplasia and its management.
Pacific Group of e-Journals (PaGe)
2015-09-02
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs453
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C54-58
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs453/pdf_42
oai:ojs.localhost:article/454
2015-10-19T19:44:18Z
aabs:CR
Asymptomatic Supplemental Premolar in a 12 year old child: A case report
Bhat, Prasanna Kumar
Supernumerary teeth are present in addition to the normal complement of teeth in permanent or deciduous dentitions. Literature reports increased occurrence of the supernumerary premolars in the mandible. A case of unilaterally impacted supplemental premolar was reported with a routine orthopantomograph view prior to the orthodontic treatment. Surgical removal was done as a prophylactic regimen.
Pacific Group of e-Journals (PaGe)
2015-09-19
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs454
Annals of Applied Bio-Sciences; Vol 2 No 3 (2015); C59-63
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs454/pdf_44
oai:ojs.localhost:article/489
2015-12-28T11:06:39Z
aabs:CR
Angiomatoid Fibrous Histiocytoma: Can it be diagnosed in uncommon locations on morphological features?
Dhameja, Neeraj
Kunwar, A
Prasad, Vikash
Goel, S C
Angiomatoid Fibrous Histiocytoma is an uncommon soft tissue tumor of uncertain histogenesis with peak incidence in younger age group. The extremeties are the commonest site though rarely it has been described in various other locations including bone. It shows certain unique histopathological and molecular features and has an indolent behaviour with recurrence in some cases and very rarely metastasis.
Pacific Group of e-Journals (PaGe)
2015-10-04
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs489
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C64-67
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs489/pdf_47
oai:ojs.localhost:article/499
2015-12-28T11:06:39Z
aabs:CR
Gestational breast cancer: a case report of two cases
Sood, Neelam
Sehrawat, Nisha
The term gestational breast cancer is defined as breast cancer diagnosed during pregnancy and up to 1 year postpartum. Overall incidence rate is 0.7 – 3.8% . These lesions are generally missed on radiology as well as cytology due to physiological and functional changes in mammary gland or misdiagnosed as hyper proliferative change of breast. These may present later in advanced stage of malignancy with axillary lymph node metastasis in 47 to 89 % of cases. Core needle biopsy is a gold standard for it’s diagnosis.. We hereby report two cases of gestational breast cancer with lymph node metastasis.
Pacific Group of e-Journals (PaGe)
2015-10-08
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs499
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C68-71
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs499/pdf_49
oai:ojs.localhost:article/501
2015-12-28T11:06:40Z
aabs:CR
Primary Ewing sarcoma of scalp diagnosed on cytology: A rare case report
Kaushik, Ankit
Sirswal, Sakshi
Gupta, Kusum
Kolte, Sachin
Arora, Disha
Primary Ewing sarcoma is small round cell tumour of neuroectodermal origin. We report a case of 16 year old female presenting with large cystic, osteolytic mass lesion in temporal region. The cytology showed loose and cohesive cluster of small round epithelial cells that were CD 99 and synaptophysin positive on immunocytochemistry.Primary scalp Ewing sarcoma is very rare, and can present with cystic lesion. FNAC along with immunocytochemistry provides early opportunity for diagnosis and treatment.
Pacific Group of e-Journals (PaGe)
2015-12-18
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs501
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C90-92
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs501/PDF%20501
oai:ojs.localhost:article/515
2015-12-28T11:06:39Z
aabs:CR
Survival in triple negative metastatic breast carcinoma
Serafimov, Aleksandar Nikola
Karakolevska-Ilova, Marija A
Joveva, Elena S. Simeonovska
Breast cancer is the most common non-skin malignancy in women, the second most common cause of cancer death, and the main cause of death in women ages 45 to 55 years. An estimated 1 million cases of breast cancer are diagnosed annually worldwide. Approximately 5-10% of patients with breast cancer have distant metastases at first presentation.The patient came to the Clinic of oncology and radiotherapy in March 2005 for further treatment with the diagnosis: Carcinoma metastaticum vertebrae lumbosacralis.Initial treatment was included 6 cycles of chemotherapy, bisphosphonate therapy and realized radiotherapy. Tumor markers at the end of treatment: CEA 238; CA15-3: 19.6. After that a radical mastectomy of the left breast with dissection of left axilla was conducted and pathological analysis showed poorly differentiated ductal invasive carcinoma (grade 3 according to Nottingham Histologic Score) with immunohistochemistry findings: HER: negative, ER: negative, PR: negative or Triple negative breast cancer (TNBC).
Pacific Group of e-Journals (PaGe)
2015-10-25
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs515
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C72-74
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs515/pdf_51
oai:ojs.localhost:article/516
2015-12-28T11:06:39Z
aabs:CR
Primary Epithelioid Sarcoma of Forearm with Axillary Lymphnode Metastasis: A Rare case report
Kshatriya, Ankur Singh
Gupta, Nisha
Vaishnav, Mitsu
Garg, Sameep
Primary epithelioid sarcoma is a rare, slow growing malignant mesenchymal tumour, which may mimics a benign granulomatous lesion clinically and cytologically, leading to misdiagnosis. This is typically present as a subcutaneous or deep dermal mass in distal portions of the extremities with strong propensity for local recurrence and metastasis. Cytologically it is very challenging to diagnose epithelioid sarcoma as it may mimics synovial sarcoma, malignant melanoma, squamous cell carcinoma and epithelioid angiosarcoma. In this report we are describing the cytological features of epithelioid sarcoma with emphasizing on FNAC as the first line of investigation.
Pacific Group of e-Journals (PaGe)
2015-10-25
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs516
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C75-78
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs516/pdf_52
oai:ojs.localhost:article/519
2015-12-28T11:06:39Z
aabs:CR
Glucose-6-Phosphatase Dehydrogenase Deficiency: Diagnosis at Presentation
Manchanda, Jaya
Gogia, Ritu
De, Reena
Chopra, Prabhajyot
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, a most common enzyme deficiency worldwide, causes a spectrum of disease including neonatal hyperbilirubinemia with acute and chronic hemolysis. Persons with this condition also may be asymptomatic. This X-linked inherited disorder most commonly affects persons of African, Asian, Mediterranean or Middle-Eastern descent. Approximately 400 million people are affected worldwide. This is a case of a 37 year old man who presented with a typical clinical and haematological picture of favism. There was no initial difficulty in confirming G6PD deficiency because the enzyme concentrations were compatible with heterozygosity for G6PD deficiency. It is uncommon for the patient to present with low G6PD level at presentation; hence this case is being reported.
Pacific Group of e-Journals (PaGe)
2015-11-06
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs519
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C79-82
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs519/pdf_55
oai:ojs.localhost:article/559
2015-12-28T11:06:40Z
aabs:CR
The hidden parasite in palpable nodule: Cysticercosis on cytology
Mittal, Ankur
Gupta, Ruchi
Selhi, Pavneet
Kaur, Harpreet
Sood, Neena
Cysticercosis is the most common parasitic infection of soft tissue. It is more common in northern parts of India. Fine needle aspiration cytology (FNAC) is a useful and rapid technique in the diagnosis of Cysticercosis We report a case of cysticercosis in a 27-year-old female patient, who presented with a subcutaneous swelling in the right arm which was diagnosed on FNAC. FNAC in cysticercosis is a low-cost outpatient procedure. It is one of the tools for preoperative diagnosis which obviates the need for open biopsy
Pacific Group of e-Journals (PaGe)
2015-12-15
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs559
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C87-89
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs559/pdf_65
oai:ojs.localhost:article/575
2015-12-28T11:06:39Z
aabs:CR
Cytodiagnosis of Chondrosarcoma: A case report
Patki, Swati
Kumavat, Prashant
Khedekark, Kavita
Gadgil, Nitin
Chaudhari, Chetan
Primary tumors involving the bony skeleton of the chest wall are uncommon. Chondrosarcomas of thorax are unusual tumors categorized as axial malignancies that invade and destroy the adjacent bone. Fine needle aspiration cytology (FNAC) is effective in the diagnosis of bone tumors when combined with careful radiologic and clinical evaluation. Chondrosarcomas often arise in the pelvis or bones of the trunk, but primary chest wall (rib) chondrosarcomas are relatively rare. Incidence of chondrosarcoma peaks in the 5th to 6th decade. We present a two cases one of 58-year-old male with anterior chest wall mass and another of 70-year-old male presented with anterolateral chest wall mass. Fine needle aspiration was done and smear studied showed increased cellularity with chondromyxoid background and tissue fragment with chondrocytes showing anisonucleosis and nuclear pleomorphism. Few binucleate cells were seen and few nuclei showed prominent nucleoli. The diagnosis of chondrosarcoma was considered.
Pacific Group of e-Journals (PaGe)
2015-12-11
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs575
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C83-86
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs575/pdf_64
oai:ojs.localhost:article/584
2015-12-28T11:06:40Z
aabs:CR
Primary Synovial Sarcoma Kidney: A Rare Case Report
Singh, Neha
Chauhan, Jitender Singh
Primary synovial sarcoma (PSS) of the kidney is a rare entity. Since morphologic differentiation from other tumors like metastatic sarcoma, sarcomatoid renal cell carcinoma, retroperitoneal liposarcoma may be difficult, other diagnostic modalities like immunohistochemistry, cytogenetic & advanced molecular analyses need to be employed.Despite its rarity & non specific presentation, pathologist and clinicians should consider synovial sarcoma in the differential diagnosis of renal masses for the proper management of patients, especially when histopathological examination shows malignant spindle cell neoplasm of kidney.
Pacific Group of e-Journals (PaGe)
2015-12-28
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs584
Annals of Applied Bio-Sciences; Vol 2 No 4 (2015); C93-96
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs584/pdf_66
oai:ojs.localhost:article/594
2016-04-01T19:07:17Z
aabs:CR
Diagnosis of primary abdominal wall endometriosis on cytology: An unusual presentation
Kaushik, Ankit
Jaiswal, Anamika
Abdominal wall endometriosis is a rare type of extra pelvic endometriosis. The abdominal wall endometriosis mostly occurs in the pre existing laprotomy scars in the lower abdominal wall following caesarian section or hysterectomy. We present a case of primary abdominal wall endometriosis in arising in the anterior abdominal wall above umbilicus with no previous history of any surgery or scar, diagnosed on fine needle aspiration cytology. Primary abdominal wall endometriosis is extremely rare and can be clinically challenging, Fine needle aspiration cytology provides easy and reliable technique for diagnosing endometriosis.
Pacific Group of e-Journals (PaGe)
2016-01-02
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
application/vnd.openxmlformats-officedocument.wordprocessingml.document
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs594
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C1-3
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs594/pdf_67
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs594/970
oai:ojs.localhost:article/704
2016-04-01T19:07:17Z
aabs:CR
A Diagnostic Dilemma of Nasal Meningo-encephalocele: a case report
Sharma, Ritu
Gupta, Vivek
Kumar, Gaurav
Nasal Meningo-encephalocele present at birth as congenital deformity with characteristic swelling over the nose. Atypical nasal encephaloceles are usually missed at birth due to absence of any external swelling and they present with diagnostic difficulties. We describe a case of congenital nasal swelling present at the root of nose in a 1 year old male child who underwent FNAC procedure followed by radio diagnostic approach and diagnosed as a case of Meningo-encephalocele in a Pathology department. An encephalocele is a rare disorder, caused by failure of the neural tube to close completely during fetal development. A meningocele is an encephalocele that contains only the meninges and cerebral spinal fluid (CSF).
Pacific Group of e-Journals (PaGe)
2016-02-29
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
application/vnd.openxmlformats-officedocument.wordprocessingml.document
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs704
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C4-7
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs704/pdf_86
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs704/1008
oai:ojs.localhost:article/742
2016-04-01T19:07:17Z
aabs:CR
Peutz-Jegher's syndrome: A diagnosis clinched on histopathology
Chowdhury, Somshamkar
Tyagi, Neha
Dawson, Leelawathi
Mandal, Ashish K
Peutz Jeghers syndrome (PJS) is an inherited autosomal dominant disorder characterised by hamartomatous polyp in the gastrointestinal tract and pigmented mucocutaneous lesion. Data on prevalence of PJS in India is not available. PJS predisposes sufferers to various malignancies (gastrointestinal, pancreatic, lung, breast, uterine, ovarian and testicular tumours).we report here a case of 18 year old male with Peutz Jeghers syndrome.
Pacific Group of e-Journals (PaGe)
2016-03-09
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs742
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C8-12
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs742/pdf_91
oai:ojs.localhost:article/760
2016-04-01T19:07:17Z
aabs:CR
Ruptured Ovarian Pregnancy in a Young Primigravida
Singh, Beant
Kaur, Balwinder
Kaur, Parneet
Gupta, Ramiti
Primary ovarian pregnancy is one of the rarest variety of ectopic pregnancy accounting for 0.15-3% of all ectopic gestations. Heartig estimated that ovarian pregnancy occur in 1 in 25000-40000 pregnancies. Pre operative diagnosis is challenging and needs high index of suspicion. In any case of ruptured ectopic pregnancy where tubes are found to be normal on laparotomy an ovarian pregnancy must be ruled out. We report such a rare case of ruptured ovarian pregnancy diagnosed on laparotomy which was later on confirmed by histopathological examination
Pacific Group of e-Journals (PaGe)
2016-03-23
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs760
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C13-15
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs760/pdf_94
oai:ojs.localhost:article/761
2016-04-01T19:07:17Z
aabs:CR
Pure mucinous carcinoma of male breast: case report of a rare histological subtype of male breast carcinoma
Deka, Riju Rani
Ahmed, Shiraj
Handique, Amitabh
Introduction: Male breast carcinoma is are rare malignancies occurring in older males and are of aggressive in nature, presenting in an advanced stage. Rarity and deviation from usual reported biological characteristics led us to report this case of pure mucinous carcinoma of male breast. Case report: A 52 years old male presented with a mass below areola found adhered to overlying skin. Resected mass was lobular 5 cm which on cut section was multiloculated filled with mucinous fluid. H&E stain from sections from different area showed features of pure mucinous carcinoma of breast with clear cut margins. Immunohistochemical examination showed nuclear positivity for ER receptor and negative for PR receptor, and membrane did not stain for HER2/neu receptor.Conclusion: More of this rare subtype of male breast carcinoma with its varied biological characteristics should be reported to know more about its biological course so that improvement in the treatment options and steps for its prevention can be taken.
Pacific Group of e-Journals (PaGe)
2016-03-23
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs761
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C16-20
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs761/pdf_95
oai:ojs.localhost:article/772
2016-04-01T19:07:17Z
aabs:CR
Early Gastric carcinoma: A rare variant of a common entity.
Trisal, Monal
Sengar, Kangana
Kotwal, Sumedha
Deb, Sanjay
Dawar, Ramesh
Gastric Carcinoma is the leading cause of cancer death worldwide. Gastric cancer confined to the mucosa and submucosa is regarded as early gastric cancer due to its overall favourable prognosis. Although common in Japan, early gastric cancer is an infrequent occurrence in India. Endoscopist should be more suspicious about these lesions as these can be easily neglected.
Pacific Group of e-Journals (PaGe)
2016-03-23
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
application/msword
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs772
Annals of Applied Bio-Sciences; Vol 3 No 1 (2016); C21-24
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs772/pdf_96
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs772/1022
oai:ojs.localhost:article/785
2016-07-22T18:20:32Z
aabs:CR
Sudipta Kar’s Modification of Guide Flange Prosthesis for mandibular repositioning
Kar, Sudipta
The unilateral surgical removal condyle due to irreparable traumatic injury may result in mandibular deviation towards the surgical side and ultimately causes unstable occlusion. Unilateral condylectomy may also result in impaired speech articulation, and facial disfigurement. A corrective device known as 'guide flange prosthesis' is used to limit this manifestation. Restoration of acceptable functional occlusion is one of the goals of our treatment modality. Dentition can be used to confirm proper realignment of the mandibular deviation. This can be achieved by the use of guide flange prosthesis. This case report delineates the rehabilitation of a paediatric patient having deviation of the mandible following condylectomy using maxillary guide flange prostheses. Guide flange prosthesis can be considered as a training device. It guides the patient to reposition the mandible into the proper intercuspal position.
Pacific Group of e-Journals (PaGe)
2016-04-08
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
application/msword
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs785
Annals of Applied Bio-Sciences; Vol 3 No 2 (2016); C25-29
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs785/pdf_98
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs785/1035
oai:ojs.localhost:article/788
2016-07-22T18:20:32Z
aabs:CR
Peripheral Ossifying Fibroma : A case report
Purkait, Soumya
Bandyopadhyay, Prasanta
Mallick, Bakul
Das, Indrasri
Das, Dipayan
Peripheral ossifying fibroma (POF) is a reactive lesion of the gingival tissue that predominantly affects women. It originates from the cells of the periodontal ligament. The definitive diagnosis is established by histological examination. In this article, we have presented a case report with the histopathological evaluation and management.
Pacific Group of e-Journals (PaGe)
2016-04-12
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs788
Annals of Applied Bio-Sciences; Vol 3 No 2 (2016); C30-33
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs788/pdf_99
oai:ojs.localhost:article/850
2016-07-22T18:20:32Z
aabs:CR
Management of Aberrant Frenum: series of cases
Bagchi, Suchi Suvra
Sarkar, Puja
Bandyopadhyay, Prasanta
The frenum is a mucous membrane fold that attaches the lip and the cheek to the alveolar mucosa, the gingiva, and the underlying periosteum. A frenum that encroaches on the margin of the gingiva may interfere with plaque removal and cause tension. Frenectomy is the complete removal of the frenum that can be made by scalpels or with soft tissue lasers. This article describes 3 case reports of different frenectomy techniques used for management of aberrant frenum.
Pacific Group of e-Journals (PaGe)
2016-05-12
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
application/vnd.openxmlformats-officedocument.wordprocessingml.document
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs850
Annals of Applied Bio-Sciences; Vol 3 No 2 (2016); C34-39
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs850/pdf_106
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs850/1051
oai:ojs.localhost:article/883
2016-07-22T18:20:32Z
aabs:CR
Adenomyoepithelioma arising in axillary breast tissue: a diagnostic rarity: case report with literature review
Lahori, Mega
Gupta, Sakul
Raina, Bawana
Khajuria, Arvind
Adenomyoepithelioma is an uncommon, benign tumor of biphasic nature which arises from myoepithelial and epithelial cells. It has been recognized mainly in breast tissue, along with skin adnexa, lungs and salivary glands. The typical histologic appearance consists of acinar structures composed of an inner layer of epithelial cells with eosinophilic cytoplasm and a prominent peripheral layer of myoepithelial cells with clear cytoplasm. Prognosis of patients with AME is usually good, but it has a potential for local recurrence and rarely, malignant transformation with distant metastases to lung, brain, and liver. We present the rare case of a 42 year old female with left sided axillary lump that was diagnosed as adenomyoepithelioma arising from accessory breast tissue in the axilla. This of interest not only because of the rarity of the lesion, but also due to the peculiarity of its origin from accessory mammary gland tissue of axillary location.
Pacific Group of e-Journals (PaGe)
2016-06-01
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs883
Annals of Applied Bio-Sciences; Vol 3 No 2 (2016); C40-43
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs883/pdf_113
oai:ojs.localhost:article/920
2016-07-22T18:20:32Z
aabs:CR
Rare case of Ovarian Ectopic Pregnancy
Joshi, Shikha
Agrawal, Dipti
Fotedar, Sunita
Ovarian pregnancy is a rare form of ectopic pregnancy. It constitutes to 1% of all ectopic pregnancies which usually ends with rupture before the end of the first trimester.We report here one such uncommon case of ovarian ectopic pregnancy. 38 years old P2L2 woman with one previous cesarean section and one VBAC with history of IUCD for 5 years presented with hypovolemic shock. During laparotomy, ruptured right ovarian ectopic pregnancywith 1.5 litres of haemoperitoneum was found , and wedge resection of the ovary was done. Histopathological examination confirmed it to be an ovarian ectopic pregnancy.Intra uterine devices (IUD) is one of contraceptive methods which prevents intra-uterine implantation in 99.5%, if implant occurs with IUD, it is tubal implantation in 95% of cases, and it is very rare in other places such as ovary. The most important risk factor of ovarian ectopic pregnancy is IUD as in this study it was showed.
Pacific Group of e-Journals (PaGe)
2016-06-15
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs920
Annals of Applied Bio-Sciences; Vol 3 No 2 (2016); C44-46
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs920/pdf_115
oai:ojs.localhost:article/928
2016-09-13T13:17:57Z
aabs:CR
Uterine Arteriovenous Malformation accidently detected: a case report
Joshi, Shikha
Agrawal, Dipti
Fotedar, Sunita
Uterine arteriovenous malformation (AVM) is a rare condition and is potentially life-threatening condition. Uterine arteriovenous malformations result from formation of multiple arteriovenous fistulous communications within the uterus without an intervening capillary network.This case report describes a 30-year-old woman with previous LSCS presented in emergency with episode of heavy vaginal bleeding with hypovolemic shock. Two weeks earlier, she had taken MTP pills for missed abortion. Transabdominal ultrasound (US) of the pelvis showed increased vascularity with multidirectional flow of the uterus with retained products .Colour Doppler was done which shows mass of size 35 mm with multiple small anaechoeic spaces in the anterior wall of cervix at the level of previous LSCS scar with increased systolic and diastolic blood flow with colour aliasing. MRI findings of an AVM include a focal uterine mass that consists of a group of distinct, serpiginous flow voids on T2W imaging. Beta HCG was 30mIU/mL. Patient was referred to higher centre for embolization of AVM which was performed successfully.
Pacific Group of e-Journals (PaGe)
2016-07-28
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs928
Annals of Applied Bio-Sciences; Vol 3 No 3 (2016); C47-49
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs928/pdf_122
oai:ojs.localhost:article/958
2016-09-13T13:17:57Z
aabs:CR
Amlodipine induced chylous ascites in a patient undergoing peritoneal dialysis: A case report
Gupta, Sakul
Lahori, Mega
Bhat, Sanjay
Amlodipine besilate, long-acting dihydropyridine type calcium channel blocker is widely used as an antihypertensive agent. In some reports, long-acting dihydropyridine type calcium channel blockers caused chylous ascites in peritoneal dialysis patients but none of the cases was associated with use of amlodipine. Here, we describe a case of a patient who was on peritoneal dialysis for CKD and developed chylous ascites after he was prescribed amlodipine for hypertension. The chylous ascites resolved after cessation of amlodipine therapy. The exact mechanism of this phenomenon is still not established although few speculative theories are known. A thorough clinical, laboratory and imaging assessment of this patient didn’t suggest any alternative diagnosis. We conclude that this patient’s chylous ascites was amlodipine related and physicians should be aware of the possibility of ascites due to the administration of long-acting dihydropyridine type calcium channel blockers particularly in those undergoing peritoneal dialysis.
Pacific Group of e-Journals (PaGe)
2016-08-18
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs958
Annals of Applied Bio-Sciences; Vol 3 No 3 (2016); C50-52
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs958/pdf_127
oai:ojs.localhost:article/1010
2016-09-13T13:17:57Z
aabs:CR
Post-coital Acute Rectovaginal fistula: a rare case report
Jain, Puja
Saini, Rashmi
Most case of Rectovaginal fistula are caused by obstetric injuries, surgical complications, infections and rarely may follow coital Acts. Postcoital non obstetric vaginal laceration due to consensual sexual Act are generally minute mucosal tears and generally heal by themselves, but in some cases, the vaginal mucosa is lacerated deeper and bleeding may require suturing of open vessels. The aim of this case report is to highlight a rare case of acute low rectovaginal fistula which a 25 yrs old women developed by penile penetration through the full thickness of rectovaginal wall after consensual intercourse and its management in emergency settings.
Pacific Group of e-Journals (PaGe)
2016-08-21
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1010
Annals of Applied Bio-Sciences; Vol 3 No 3 (2016); C53-55
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1010/pdf_130
oai:ojs.localhost:article/1060
2016-09-13T13:17:57Z
aabs:CR
Unruptured 14 weeks tubal ampullary pregnancy :a rare case report
Jain, Puja
Agrawal, Dipti
Fotedar, Sunita
Ectopic pregnancy is a life threatening condition and presents itself in diverse ways. Ninety five percent of ectopic pregnancies occur in fallopian tube .Ampulla is the most common site of ectopic tubal pregnancy. Diagnosis and exact location of ectopic pregnancy is usually easy during the first trimester of pregnancy by ultrasonography .However in developing countries, where resources are limited, most women do not undergo ultrasound examination during pregnancy, leading to late diagnosis. The reported average duration of diagnosis of unruptured tubal pregnancy is between 5 and 9 weeks of gestation. Rarely tubal pregnancy can remain asymptomatic and unruptured for longer duration than usual scenario. This case reports a rare case of viable, unruptured, tubal ampullary ectopic pregnancy of 14 weeks gestational age.
Pacific Group of e-Journals (PaGe)
2016-09-13
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1060
Annals of Applied Bio-Sciences; Vol 3 No 3 (2016); C56-59
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1060/pdf_133
oai:ojs.localhost:article/1066
2017-01-02T19:42:13Z
aabs:CR
Squamous Cell Carcinoma Vulva in a Young Woman
Kaur, Parmjit
Bhatia, Ruby
Singh, Aman Dev
Gupta, Ramiti
Carcinoma of vulva is an uncommon malignancy accounting for only 2% of all female genital malignancies. It is usually seen in postmenopausal women in age group ≥65 yrs. Increased life expectancy has given place to carcinoma vulva among gynaecological malignancies. However in recent years there is an increased incidence (almost doubled) of vulvar cancer in younger women. We report a case of invasive squamous cell carcinoma of vulva stage IIIb in a 36 year old woman, indeed first only in thirty years of gynaecological practical experience. The relative rarity of vulvar cancer in young age and the general lack of awareness of typical signs and symptoms even by medical professionals frequently lead to a delay in diagnosis.
Pacific Group of e-Journals (PaGe)
2016-10-04
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1066
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C60-63
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1066/pdf_134
oai:ojs.localhost:article/1082
2017-01-02T19:42:13Z
aabs:CR
Adenomatoid Tumor of Epididymis: A Case report with correlation between histology and cytology
Lahori, Mega
Gupta, Sakul
Goswami, K C
Khajuria, Arvind
Adenomatoid tumor is a rare and distinctive, benign mesothelial neoplasm of the paratesticular region in males, most commonly occurring at the tail of epididymis and constitutes 30% of paratesticular neoplasms. We present a case of adenomatoid tumor in a 35 year old male, who presented with a mass in right epididymis and was diagnosed by fine needle aspiration cytology and later confirmed on histopathology. The clinical, histopathological and cytological aspects of this rare case are discussed. FNAC plays a pivotal role in the preoperative diagnosis of these tumors as it is a simple, inexpensive, minimally invasive and reliable diagnostic modality. Due to its benign nature, the treatment of choice is local excision. We believe it is important for the physician to be aware of this interesting entity in order to make an accurate diagnosis and prevent unnecessary orchiectomy.
Pacific Group of e-Journals (PaGe)
2016-10-12
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1082
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C64-67
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1082/pdf_136
oai:ojs.localhost:article/1104
2017-01-02T19:42:13Z
aabs:CR
A Rare Case of Non Communicating Rudimentary horn with Unicornuate uterus.
Jain, Puja
Fotedar, Sunita
Raje, Suman
Daral, Rekha
Mullerian duct malformations delineate a miscellaneous group of congenital anomalies that result from the arrested development ,abnormal formation, or incomplete fusion of the mesonephric ducts. Unicornuate uterus with rudimentary horn is a rare mullerian duct anomaly of female genital tract. The frequency of this pathology is 1/100 000. It is responsible for many obstetrics and gynecological complications during reproductive life of women. These uterine anomalies are either diagnosed incidentally or the patient may present with obstetrical or gynecological problems. These patients present with dysmenorrhea,dyspareunia, and rarely chronic pelvic pain because of endometriosis and rarely with acute abdominal symptoms following distention and torsion of the non communicating rudimentary horn. We present a case of pelvic endometriosis due to non communicating but functional rudimentary horn of a uterus in a multiparous woman .
Pacific Group of e-Journals (PaGe)
2016-10-20
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1104
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C68-71
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1104/pdf_138
oai:ojs.localhost:article/1105
2017-01-02T19:42:13Z
aabs:CR
Rare site of Metastasis in Cancer Cervix: a Case Report
Khanuja, Sweta
Anand, Vijay
Cervical cancer rarely metastasizes to skin. This occurs in <2% of patients. It is more common in patients who do not receive radiotherapy after surgery but can be seen in patients after radiotherapy who have deferred taking radiotherapy by few months. We report a patient who received radiotherapy four months after surgery and remained asymptomatic for 5 months. She then noticed a lump in abdomen for which she underwent excision of the lump and it was reported as squamous cell carcinoma. The patient was concluded to have abdominal wall recurrence of cancer cervix.
Pacific Group of e-Journals (PaGe)
2016-10-27
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1105
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C72-74
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1105/pdf_139
oai:ojs.localhost:article/1131
2017-01-02T19:42:13Z
aabs:CR
Central serous chorioretinopathy leading to sub retinal bleed to postvitrectomy endophthalmitis: Diagnostic Dilemma
Khan, Balbir
Anand, Vartika Sobat
Anand, Sachin
Kashyap, Meenu
Central serous retinopathy (CSR) is a common cause of visual disturbance in the younger age group. Spontaneous visual recovery occurs in the majority of patients. A minority of patients, however, suffer permanent visual loss commonly caused by chronic retinal pigment epithelial changes. We report a devastating complication of CSR, with sub retinal haemorrhage
Pacific Group of e-Journals (PaGe)
2016-11-07
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1131
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C75-77
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1131/pdf_142
oai:ojs.localhost:article/1145
2017-01-02T19:42:13Z
aabs:CR
Solitary lymph node involvement by Langerhans Cell Hitisocytosis: Cytomorphologic diagnosis and pitfalls on Fine Needle Aspiration Cytology
Gupta, Chhaya
Gupta, Neeru
Langerhans cell histiocytosis (LCH) is a rare disease and when confined to lymph node, it is even rarer. Lymph node involvement in LCH can be seen as a component of the systemic form or it may be the initial and sometimes exclusive manifestation of the disease [1].We present a case of LCH confined to the lymph node diagnosed initially by fine needle aspiration cytology (FNAC) in a 7 year old girl. Highly cellular smears showed fair number of large histiocytic cells (langerhans cells) showing round to oval vesicular nuclei with irregular folded and grooved nuclei with abundant, pale blue cytoplasm admixed with numerous neutrophils, lymphocytes, macrophages, multinucleated giant cells and tingible body macrophages suggesting the diagnosis of LCH. This was confirmed on histopathological and immunohistochemical study of the excised lymph node. The highly characteristic common and rare cytological features are highlighted with focus on differential diagnosis and causes of pitfalls.
Pacific Group of e-Journals (PaGe)
2016-11-20
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1145
Annals of Applied Bio-Sciences; Vol 3 No 4 (2016); C78-81
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1145/pdf_143
oai:ojs.localhost:article/1279
2017-03-20T19:10:56Z
aabs:CR
Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor) masquerading clinically as malignant melanoma - A Case Report
Mondal, Ira
Chaudhuri, Arnab
Samaddar, Aparajita
Das, Nandini
Nag, Dipanwita
Bednar tumor is a rare neoplasm of intermediate malignant potential, which account for less than 5% of dermatofibrosarcoma protuberans (DFSP).This tumor is a pigmented variant of DFSP. The diagnosis is commonly made in early to mid adult life except in cases with melanin containing cells. The case report presents a 19 years old female who presented with a painless slow-growing 3.5×3×1.2 cm blackish mass on the dorsal aspect of her right foot. Histopathological examination of the biopsy specimen revealed typical features of a Bednar tumor, the diagnosis was confirmed through immunohistochemical study. DOI: 10.21276/AABS.2017.1279
Pacific Group of e-Journals (PaGe)
2017-02-03
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Case report
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1279
Annals of Applied Bio-Sciences; Vol 4 No 1 (2017); C1-3
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1279/pdf_149
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1279/1210
oai:ojs.localhost:article/1314
2017-03-20T19:10:56Z
aabs:CR
Two point fixation in zygomatic compex fractures
Sharma, Sourav
D, Vandana
Zygomatic bone along with its adjacent articulating bones is known as zygomatic complex.The zygomatic complex fractures are one of the frequently occurring maxillofacial injuries due to its prominence and facial contour. Personal altercations, Assaults, Road traffic accidents are the common causes leading to fracture of the zygomatic bone.The zygomatico-maxillary complex is one of the principle buttress of the face and helps in transmitting the occlusal forces to the skull base.Fracture of zygomatic bone may lead to aesthetic and functional deformity.There are various surgical techniques and approaches to reduce and fix the fractured zygomatic complex. Expertise of the Maxillofacial surgeon and thorough anatomical knowledge is of advantage in managing these fractures. DOI: 10.21276/AABS.2017.1314
Pacific Group of e-Journals (PaGe)
2017-02-21
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Open reduction and internal fixation,two point fixation.
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1314
Annals of Applied Bio-Sciences; Vol 4 No 1 (2017); C4-6
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1314/pdf_155
oai:ojs.localhost:article/1318
2017-07-11T18:33:54Z
aabs:CR
A Rare Case Report Of Corynebacterium minutissimum Causing Bacteremia In An Immunocompetent Patient
Gupta, Sunita
Bhargava, Vibha
Jain, Rohit
Goyal, Prateek
Gupta, G N
Non-diphtherial Corynebacteria (NDC), which are also referred to as Diphtheroids are a widely diverse collection of bacteria. Corynebacterium species are normal flora of skin and mucous membrane . Up to now, the pathogenic potential of coryneform bacteria has been underestimated. In recent years, Coryneforms have emerged as important opportunistic pathogens in immunocompromised patients. Majority of the Corynebacterium minutissimum isolates are from erythrasma. Since its discovery in 1961 Corynebacterium minutissimum is rarely implicated in bacteremia . Though routinely considered as contaminants there are reports which establish NDM as a pathogen so it should not be discarded as contaminants in general. Hereby we report a case of bacteremia due to Corynebacterium minutissimum due to polytrauma by road accident. DOI: 10.21276/AABS.1318
Pacific Group of e-Journals (PaGe)
2017-04-21
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
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image/jpeg
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https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1318
Annals of Applied Bio-Sciences; Vol 4 No 2 (2017); C13-15
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1318/pdf_181
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1318/1224
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1318/1272
oai:ojs.localhost:article/1320
2017-03-20T19:10:56Z
aabs:CR
Osteolipoma of knee: a rare case report
Chaudhuri, Arnab
Mondal, Ira
Samaddar, Aparajita
Das, Nandini
Nag, Dipanwita
Lipomas are the most common benign soft tissue tumors and appear in any part of the body. They typically consist of mature adipose tissue. Osteolipoma is an extremely rare histologic variant of lipoma that contains mature lamellar bone within the tumor and osteolipoma independent of bone tissue are very rare. We report a case of histologically confirmed osteolipoma independent of bone located just above left knee. A 61 year old female presented with medial sided left knee pain of 6 month duration. X-ray demonstrated a partially calcified 3.5 cm diameter mass located in anterior to the distal medial femur. Histologic examination of an excisional biopsy showed the lesion to be an osteolipoma. Osteolipoma is a rare histologic variant of lipoma with osseous metaplasia, but should be considered in the differential of a fat-containing neoplasm with ossification. DOI: 10.21276/AABS.2017.1320
Pacific Group of e-Journals (PaGe)
2017-02-21
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Case report
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1320
Annals of Applied Bio-Sciences; Vol 4 No 1 (2017); C7-9
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1320/pdf_156
oai:ojs.localhost:article/1332
2017-03-20T19:10:56Z
aabs:CR
Schistosomiasis of appendix with review of literature.
Mahdy, Omaia
Haider, Nazima
Fatima, Sohaila
Schistosomiasis a widespread parasitic disease is caused by a typical trematode with vertebrate-invertebrate lifecycle and occurs in well-defined geographical areas. The development of water resources and migration of populations are responsible for the introduction of the disease into new regions of the world. Schistosomiasis is an unusual cause of appendicitis. We present a case of appendicitis in a 60 year old Saudi male and discuss its review of literature.DOI: 10.21276/AABS.2017.1332
Pacific Group of e-Journals (PaGe)
2017-02-24
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Case report
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1332
Annals of Applied Bio-Sciences; Vol 4 No 1 (2017); C10-12
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1332/pdf_161
oai:ojs.localhost:article/1457
2017-07-11T18:33:54Z
aabs:CR
Lingual Schwannoma: A Case Report
Munjal, Manish
Arora, Archana
Singh, Damanpreet
Talwar, Gopika
Nagpal, Japsimran
Schwannomas are benign nerve sheath tumors uncommonly seen in the oral cavity. The etiology is largely unknown and there is no sex predilection and can occur in a vast age group. Magnetic Resonance Imaging is the investigation of choice and transoral resection allows for removal of this tumor in a vast majority of cases. Malignant transformation in these tumors is exceedingly rare. Reported here is a 2x2 cm schwannoma on the lateral border of the tongue , in a 19 yr old male for the last 8 months. Complete transoral excision with primary closure was carried out. Histopathological examination of the surgical specimen revealed features of schwannoma. DOI: 10.21276/AABS.1457
Pacific Group of e-Journals (PaGe)
2017-04-21
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1457
Annals of Applied Bio-Sciences; Vol 4 No 2 (2017); C16-17
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1457/pdf_182
oai:ojs.localhost:article/1471
2017-07-11T18:33:54Z
aabs:CR
Diagnosis of subcutaneous cysticercosis as a cystic mass over chest wall: A case report and review of the literature
Dwivedi, Tanima
Davangeri, Reshma
Cysticercosis is the common tropical disease. It is usually present as a neurocysticercosis or intramuscular lesion, rarely may it present in subcutaneous tissue in the adult age group. Prevalence of asymptomatic subcutaneous nodules in India is 12.9-38%. Subcutaneous nodule is usually occur as a part of the disseminated cysticercosis or as an isolated features. Here, we report a 45 year old male presenting with cyst over right chest wall but otherwise asymptomatic. A clinical diagnosis of epidermal cyst was made. Surgical excision was performed. Diagnosis of cutaneous cysticercosis was made by biopsy of subcutaneous nodule and patient was started on treatment. DOI: 10.21276/AABS.1471
Pacific Group of e-Journals (PaGe)
2017-05-28
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Case report
application/pdf
application/vnd.openxmlformats-officedocument.wordprocessingml.document
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1471
Annals of Applied Bio-Sciences; Vol 4 No 2 (2017); C18-20
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1471/pdf_184
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1471/1285
oai:ojs.localhost:article/1643
2017-11-24T03:57:46Z
aabs:CR
Innovative approach to lingual base lesions
Munjal, Manish
Arora, Archana
Singh, Amanjeet
Sood, Dinesh
Singla, Tushar
Visualization and resection, in toto or sampling of base tongue lesions involves either a "ceiling" or a "floor" intervention. The concerned area is not in a straight line of view, necessitating thereby either 45 or 70 degree angled telescopes with 45 or 90 degree angled punch trucut instrumentation. In addition a curved tongue retractor is needed to lift out the anterior part of the tongue. To obviate the need of one instrument, a curved blade intubation video laryngoscope can be utilized with ease. A massive base tongue hemispherical mass was excised using this innovative technique.
Pacific Group of e-Journals (PaGe)
2017-09-05
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1643
Annals of Applied Bio-Sciences; Vol 4 No 3 (2017); C21-23
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1643/pdf_192
oai:ojs.localhost:article/1663
2017-11-24T03:57:46Z
aabs:CR
A case of Synchronous Multifocus Gastric Adenocarcinoma.
Sharma, Shikha
Raina, Bawana
Rashid, Misbah
Goswami, K C
Synchronous neoplasms are defined as two or more primary tumors identified in the same patient, at the same time, in the same organ or in different organs. Here we present an interesting case of Synchronous Multifocus Gastric Adenocarcinoma with a concern that the diagnosis of synchronous multifocal gastric neoplasms can sometimes be missed during initial endoscopic investigations and during grossing sessions in histopathology units, making it obligatory for the surgeon and the histopathologist to be aware of such lesions.
Pacific Group of e-Journals (PaGe)
2017-09-05
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1663
Annals of Applied Bio-Sciences; Vol 4 No 3 (2017); C24-27
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1663/pdf_193
oai:ojs.localhost:article/1676
2017-11-24T03:57:46Z
aabs:CR
Confronting the unexpected: saddle defect during septal surgery
Munjal, Manish
Kaur, Japneet
Kaur, Amanjot
Singh, Amanjeet
Mathur, Nidhi
Munjal, Shubham
Septal surgery is aptly captioned the " bread and butter surgery " , of the ent surgeon .Sometimes in this basic surgery the unexpected happens . A septal perforation or a saddle of the cartilaginous dorsum . The former lies hidden deep inside while the latter effects the facial profile and one becomes an object of ridicule. Utilising the resected tissue or tissues from nasal vicinity one can augment the depression . Introduction . In certain septal deformities ,the inferior border of the quadrangular cartilage overrides the premaxillary and the maxillary crest ,thereby producing a sharp or a blunt spur. Resection of the same with a " antero -posterior chondrotomy" attains a good nasal patency . A jutting premaxillary or maxillary crest is amenable to a similarly oriented " osteotomy " . DOI: 10.21276/AABS.1676
Pacific Group of e-Journals (PaGe)
2017-10-01
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1676
Annals of Applied Bio-Sciences; Vol 4 No 3 (2017); C28-30
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1676/pdf_194
oai:ojs.localhost:article/1678
2017-11-24T03:57:46Z
aabs:CR
Submandibular haemangioma involving parotid tail - Case report
Munjal, Manish
Puri, Sanjeev
Kaur, Japneet
Kaur, Amanjot
Rishi, Porshia
Munjal, Shubham
Singh, Anmol
Fasciocervical haemangiomas present as a doughy swelling in the submandibular or the parotid region. Imaging studies preferably the MRI clinch the diagnosis with areas of vascular voids. A rare case of haemangioma interposed between the tail of parotid and submandibular gland was delivered from the upper presternomastoid gutter. DOI: 10.21276/AABS.1678
Pacific Group of e-Journals (PaGe)
2017-10-01
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1678
Annals of Applied Bio-Sciences; Vol 4 No 3 (2017); C31-33
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1678/pdf_195
oai:ojs.localhost:article/1801
2017-12-24T02:07:23Z
aabs:CR
Paramedian forehead flap in post Radiotherapy fistula
Munjal, Manish
Kaur, Japneet
Tilavat, Venus
Kaur, Amanjot
Munjal, Shubham
The medial canthal fistula gains notoriety for its unsuccessful “ repair “ utilising the varied flaps from its vicinity . Ultimately the conventional forehead flap is lone “ saviour “ in this malady
Pacific Group of e-Journals (PaGe)
2017-12-24
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1801
Annals of Applied Bio-Sciences; Vol 4 No 4 (2017); C34-37
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/aabs1801/pdf_206
oai:ojs.localhost:article/2064
2018-06-24T14:57:27Z
aabs:CR
Fnac of Rosai - Dorfman Disease - Report of 5 Cases
Dhameja, Neeraj
Chaudhary, Deepshikha
Bharti, Shreekant
Awasthi, Chakrapani
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare non malignant histiocytic proliferative disorder of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.Very few cases has been diagnosed on FNAC. Here we report 5 cases of Rosai – Dorfman disease presenting with massive bilateral cervical lymphadenopathy. Hence FNAC is a useful and reliable tool for the diagnosis of Rosai-Dorfman disease due to which biopsy can be avoided in these patients.
Pacific Group of e-Journals (PaGe)
2018-06-24
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2064
10.21276/aabs.2064
Annals of Applied Bio-Sciences; Vol 5 No 2 (2018); C4-6
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2064/1506
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/2167
2018-06-20T01:31:43Z
aabs:CR
Steroid Cell Tumor: A Rare Ovarian Tumor
Raheja, Aastha
Goswami, Deepti
Sakhija, Pooja
Gandhi, Gauri
Singhla, Bidhisha
Ovarian steroid cell tumors are sex-cord stromal tumors that arise from lutein cells or leydig cells. These are very rare- accounting for<0.1% of all ovarian tumors.. Some of these tumors may be functional and secrete hormones. Nearly 56-77% of the cases present withhyperandrogenism. Rarely steroid cell tumors may arise in the adrenal cortex from the adrenal rest cellsWe report a case of a 60-year old lady who presented with gradual onset abdominal distension for two years. She had no other complains andhad undergone hysterectomy 20 years back. Her abdomen was over distended due to a large, tense cystic, non-tender mass. Imaging studiesrevealed a large, mainly cystic abdominopelvic mass; however its origin could not be made out. The left adrenal gland was found to be bulkybut morphologically normal. Serum DHEAS levels were normal thus ruling out adrenal pathology. Serum levels of CA 125 and CEA were alsonormal. Exploratory laparotomy was done. A large thin walled cyst occupied the pelvis and abdomen. . It measured 25x20x16cm and contained4.2 litre of straw colored fluid. The fluid was drained and the entire cyst wall was excised. Ovaries were not visualized. Frozen section report ofthe cyst wall was suggestive of a neuroendocrine tumor. Final histopathology report was of benign steroid cell tumor not otherwise specified.In view of the benign nature of ovarian pathology, no further intervention was required. The patient had an uneventful postoperative recover.
Pacific Group of e-Journals (PaGe)
2018-06-08
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2167
10.21276/aabs.2167
Annals of Applied Bio-Sciences; Vol 5 No 2 (2018); C1-3
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2167/1478
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/2390
2021-04-09T18:30:31Z
aabs:CR
A Rare Case of Carney's Complex in an Adult
Singh, Sonal
Mujeeb, V R
Jambunathan, Prashant
A 35 year old male came to medical attention when he was seen to have prominent jaw with frontal bossing and large doughy hands. Clinical examination revealed features of acromegaly and multiple lentiginous hyper-melanotic patches on the upper and lower extremities. Imaging revealed multiple left atrial myxomas and a diffusely enlarged adenohypophysis. A diagnosis of Carney's Complex was made, which is a rare autosomal dominant condition, characterized by the triad of endocrinopathies, atrial myxomas and lentiginous skin lesions. He was surgically managed for the same and is currently asymptomatic. He continues to remain under regular follow up at our centre. With about 150 described cases on contemporary literature1, this rare condition, often requiring a multidisciplinary approach for accurate management, remains both a therapeutic challenge and an enigma.
Pacific Group of e-Journals (PaGe)
2021-04-09
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2390
10.21276/aabs.2390
Annals of Applied Bio-Sciences; Vol 7 No 1 (2021); C6-8
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2390/1985
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/2749
2021-04-09T18:30:31Z
aabs:CR
Spontaneous Complete Resolution of Significant Volume Extradural Haematoma: A Case Report
Sharma, Krishan Kumar
Ali, Asgar
According to brain Trauma foundation guidelines, any extradural hematoma with volume more than 30 ml should undergo surgical evacuation regardless of the Glasgow Coma Scale (GCS). Patient presented was neurologically normal with mild headache, his CT Scan Head showed left parietal extradural hematoma (volume7.35x2.37x7.1=50cc). The patient was kept under regular clinico-radiological assessment. In ten weeks, duration, it showed complete resolution of extradural hematoma. This support it as rationalized treatment approach for such cases before surgery. Which will reduce workload on busy Neurosurgical operation theatre and surgical complications, also reduce expenditure on health care.
Pacific Group of e-Journals (PaGe)
2021-04-09
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2749
10.21276/aabs.2749
Annals of Applied Bio-Sciences; Vol 7 No 1 (2021); C4-5
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2749/1987
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/2993
2020-12-20T06:35:39Z
aabs:CR
Intravascular Papillary Endothelial Hyperplasia (Masson’s Tumor) of Wrist
Yadav, Shakti Kumar
Yadav, Alka
Naeem, Roshina
Singh, Sompal
Sarin, Namrata
Pruthi, Sonam Kumar
Nonspecific slow growing lesions of hand and wrist can be difficult to diagnose. We present a case of intravascular papillary endothelial hyperplasia (IPEH), or Masson’s tumor of the wrist. Present case is a 23-year-old female presented with a vague, soft, mobile and mildly tender swelling over the ventral aspect of the right wrist. The present case highlights the importance of excision and histopathological examination along immunohistochemistry in these lesions.
Pacific Group of e-Journals (PaGe)
2020-12-20
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2993
10.21276/aabs.2993
Annals of Applied Bio-Sciences; Vol 6 No 1 (2020); C1-3
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/2993/1941
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/3019
2021-04-09T18:30:31Z
aabs:CR
Malakoplakia of Testis: A Case Report
Machiwal, Kishan
Porwal, Vandana
Tanwar, Soniya
Kasliwal, Neena
Malakoplakia is an uncommon chronic inflammatory disease usually affecting the urogenital tract and often associated with the infection due to coliform bacteria (E. coli). It is characterised by the presence of VonHansemann cells and intracytoplasmic inclusion bodies called Michaelis-Gutmann Bodies. This condition is common in bladder (40%), Testes are affected in 12% cases. The lesion mainly occurs in middle aged men, appearing clinically as epididymo-orchitis or testicular enlargement with fibrous consistency and some soft areas. Orchidectomy is the only way to differentiate from epididymoorchitis or infected processes and testicular malignancy. This is a case report of an elderly patient with testicular malakoplakia
Pacific Group of e-Journals (PaGe)
2021-04-09
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/3019
10.21276/aabs.3019
Annals of Applied Bio-Sciences; Vol 7 No 1 (2021); C1-3
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/3019/1986
http://creativecommons.org/licenses/by-nc/4.0
oai:ojs.localhost:article/3039
2021-06-29T10:26:44Z
aabs:CR
Androgen Insensitivity Syndrome (Testicular Feminization) – A Retrospective Diagnosis: Case Report
Singh, Ankur
Tanwar, Soniya
Porwal, Vandana
Kasliwal, Neena
Testicular feminization, or the androgen insensitivity syndrome, is a rare disease. It occurs due to various abnormalities of the X chromosome, a male, genetically XY, has some physical characteristics of a female or a full female phenotype. The androgen insensitivity syndrome occurs because of a resistance to the actions of the androgen hormones, which in turn switches the development towards the aspect of a female. We report a retrospectively diagnosed case of complete androgen insensitivity syndrome in a 50 years old woman who presented with right inguinal swelling. We aim to improve our knowledge of this illness from the data that provides us this study.
Pacific Group of e-Journals (PaGe)
2021-06-29
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
application/pdf
https://www.pacificejournals.com/journal/index.php/aabs/article/view/3039
10.21276/aabs.3039
Annals of Applied Bio-Sciences; Vol 7 No 1 (2021); C9-11
2349-6991
2455-0396
eng
https://www.pacificejournals.com/journal/index.php/aabs/article/view/3039/2003
http://creativecommons.org/licenses/by-nc/4.0