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A Giant primary mesenteric Liposarcoma in an adolescent male: A rare case with presentation in unusual age and location 一例青少年男性巨大原发性肠系膜脂肪肉瘤:罕见的病例，表现在不寻常的年龄和位置
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.10
V. Rana, Ranjan Praveer, Singh Giriraj, Rathi Khushi Ram
{"title":"A Giant primary mesenteric Liposarcoma in an adolescent male: A rare case with presentation in unusual age and location","authors":"V. Rana, Ranjan Praveer, Singh Giriraj, Rathi Khushi Ram","doi":"10.5530/OGH.2017.6.1.10","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.10","url":null,"abstract":"Primary mesenteric Liposarcoma is a rare neoplasm and only few documented cases are there in literature that too in adults. We report a case of giant primary mesenteric Liposarcoma in an adolescent male. Our patient is a 17 yrs old male who presented with gradual abdominal distension and was found to have huge multilobated and heterogeneous abdominal tumor arising from transverse mesocolon on imaging. The excised tumor weighed 19 kg and was reported as well differentiated Liposarcoma (WDLPS) on histomorphology. Atypical Lipomatous Tumor and WDLPS are synonyms describing lesions that are identical morphologically, karyotypically and in terms of biological potential. In deep visceral sites where wide excision margin are difficult to attain, the term WDLPS is preferred. Myxoid Liposarcoma is the most common variant of LPS seen in children and young adults with lower extremities being commonest site of occurrence. Our case is unique in rarity of lesion, its dimensions, location and uncommon histomorphology for age.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127142664","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A Rare Case of a Diffuse Large B-Cell Lymphoma (DLBCL) arising From The Parotid Gland In a Patient With Sjogren’s Syndrome 一例罕见的弥漫大b细胞淋巴瘤(DLBCL)起源于腮腺的干燥综合征患者
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.6
Suresh Babu Mallekavu Chikkadasappa, G. Kanakasetty, Rajeev Lakkavalli Krishnappa, S. Rao
{"title":"A Rare Case of a Diffuse Large B-Cell Lymphoma (DLBCL) arising From The Parotid Gland In a Patient With Sjogren’s Syndrome","authors":"Suresh Babu Mallekavu Chikkadasappa, G. Kanakasetty, Rajeev Lakkavalli Krishnappa, S. Rao","doi":"10.5530/OGH.2017.6.1.6","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.6","url":null,"abstract":"Primary lymphoma of the salivary gland is rare, with NHL being 5% of all extra nodal lymphomas and 2% of all salivary gland tumors. Most are low grade lymphomas with MALT lymphomas being the most common. DLBCL lymphomas are uncommon with most thought to be due to transformation from underlying low-grade lymphomas, postulated to arise in those with sialedinitis and Sjogren’s syndrome. We report a rare case of DLBCL in a patient on treatment for Sjogren’s Syndrome.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"11 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131622642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
CT Findings in a rare case of Esophageal Mucocele Involving entire Native Esophagus 食道黏液囊肿累及整个食道的罕见CT表现
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.12
P. Garg, Raju Sharma, Madhu Dayal
{"title":"CT Findings in a rare case of Esophageal Mucocele Involving entire Native Esophagus","authors":"P. Garg, Raju Sharma, Madhu Dayal","doi":"10.5530/OGH.2017.6.1.12","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.12","url":null,"abstract":"","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"21 5 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123508572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Unusual Initial Presentation of Hepatocellular Carcinoma: Skeletal Metastases 肝细胞癌不寻常的初始表现:骨骼转移
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.3
Sonal Saran, P. Khera, R. Rajagopal, Neeraj Mehta, P. Elhence
{"title":"Unusual Initial Presentation of Hepatocellular Carcinoma: Skeletal Metastases","authors":"Sonal Saran, P. Khera, R. Rajagopal, Neeraj Mehta, P. Elhence","doi":"10.5530/OGH.2017.6.1.3","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.3","url":null,"abstract":"Skeletal metastases from Hepatocellular carcinomas are rare and very rarely present as the initial symptom. We therefore report a case with multiple exclusively skeletal metastatic masses from hepatocellular carcinoma in a patient with no prior history of chronic liver disease.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125260541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adult Wilms Tumour: Rare case report with an exceptional survival in metastatic disease 成人肾母细胞瘤:罕见病例报告，在转移性疾病中有特殊的生存
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.8
Kabre Rs, Kamble Km
{"title":"Adult Wilms Tumour: Rare case report with an exceptional survival in metastatic disease","authors":"Kabre Rs, Kamble Km","doi":"10.5530/OGH.2017.6.1.8","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.8","url":null,"abstract":"Incidence of wilms tumour(WT) in adults is low, the exact number is unknown owing to insufficient documentation or incorrect diagnosis. Compared to their paediatric counterparts, adult wilms tumour has shown poorer prognosis, but with use of multi-modality treatment there is improvement in response and overall survival. Here in this case report we discuss a case of adult wilms tumour with characteristic triphasic histology & unusual 3 year survival post operatively with irregular treatment in the face of metastatic disease.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126633819","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recurrent Extramammary Paget’s disease of Axilla: A case report 复发性腋窝乳腺外佩吉特病1例
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.9
M. Rasool, Najmi Arshad Manzoor, Shareefa Akhter, Bhat Altaf Rasool, S. A. Bashir
{"title":"Recurrent Extramammary Paget’s disease of Axilla: A case report","authors":"M. Rasool, Najmi Arshad Manzoor, Shareefa Akhter, Bhat Altaf Rasool, S. A. Bashir","doi":"10.5530/OGH.2017.6.1.9","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.9","url":null,"abstract":"Extramammary Paget’s disease of axilla is extremely rare and has not been well reported. It can be confused with eczema, superficial spreading melanoma or contact dermatitis. These patients can have an underlying malignancy. We report one such case in a 65 year old female who presented with recurrence of the lesion after 6 years.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"16 8","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114106874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Celiac Disease: A Scientometric Analysis of World Publication Output, 2005-2014 乳糜泻:2005-2014年世界出版物产出的科学计量分析
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.2
Madhu Bansal, Ritu Gupta, Jivesh Bansal
{"title":"Celiac Disease: A Scientometric Analysis of World Publication Output, 2005-2014","authors":"Madhu Bansal, Ritu Gupta, Jivesh Bansal","doi":"10.5530/OGH.2017.6.1.2","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.2","url":null,"abstract":"International license. Cite this article: Bansal M, Gupta R, Bansal J. Celiac Disease: A Scientometric Analysis of World Publication Output, 2005-2014. OGH Reports. 2017;6(1):8-15. ABSTRACT The paper presents an analysis of 14317 world papers in celiac disease, retrieved from Scopus database for the period 2005-14, experiencing an annual average growth rate of 5.20% and citation impact of 12.53.The 15 most productive countries account for 83.89% share in world output, with largest share (21.40%) coming from U.S.A, followed by Italy (12.61%), U.K. (8.23%), Germany (5.41%) etc., during 2005-14. U.S.A achieved the global citation share (35.13%) followed by Italy (17.16%), U.K. (15.74%) etc. Medicine registered the highest publication share (87.93%), followed by biochemistry, genetics and molecular biology (13.56%), immunology and microbiology (6.73%), agricultural and biological sciences, (5.57%), nursing (3.07%), pharmacology, toxicology and pharmaceutics (2.74%), neurosciences (2.26%), etc. Diarrhoea contributed the largest share (8.10%) in publications by symptoms during 2005-14, followed by abdominal pain (7.68%), insulin dependent diabetes mellitus (6.84%), Crohn disease (6.22%), enteritis (5.34%), etc. Gluten free diet contributed the largest share (18.47%) among significant keywords. The 15 most productive organisations, authors and journals accounted for 15.06%, 10.71% and 16.57% share of the world publication output respectively during 2005-14. It is concluded that individual countries must foster global research and development, by way of providing increased investment in R and D and increase their specialized manpower and provide adequate training courses and infrastructural facilities to scientists and researchers to control the challenges faced by the spread of this disease.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"462 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127147315","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Cardiac Cirrhosis–An Uncommon Manifestation of Common Disease 心脏肝硬化——常见病的罕见表现
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.7
J. Khare, Prachi Srivastava, J. Wadhwa, P. Deb
{"title":"Cardiac Cirrhosis–An Uncommon Manifestation of Common Disease","authors":"J. Khare, Prachi Srivastava, J. Wadhwa, P. Deb","doi":"10.5530/OGH.2017.6.1.7","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.7","url":null,"abstract":"Background: Chronic Right Heart failure is known to cause Liver Cirrhosis but it is rare. Here we are reporting the case of cardiac cirrhosis presented to us with signs of Liver Failure. Case Report : 50 year male, farmer, chronic smoker presented with progressive abdominal distension and episodes of malena since 6 months and an episode of hematemasis. On work up Liver cirrhosis was diagnosed but cause for cirrhosis was not established and on general examination pulse was irregular and features of pulmonary hypertension were present. On reviewing he revealed history of chronic cough and breathlessness with winter exacerbations and pedal edema. Chest X-ray suggested cardiomegaly, ECG suggested low voltage complex with poor R wave progression and 2-D Echo suggested pulmonary hypertension with tricuspid regurgitation with right sided dysfunction suggesting cardiac cause for cirrhosis. Conclusion : Chronic Right Heart Failure is known but rare cause of Liver cirrhosis.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"29 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125866354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Masquerading Adenoid cystic Carcinoma of Trachea. A case report 伪装性气管腺样囊性癌。病例报告
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI: 10.5530/OGH.2017.6.1.4
Bhushan Kathuria, M. Pareek, S. Kadam, Rigved nitala
{"title":"Masquerading Adenoid cystic Carcinoma of Trachea. A case report","authors":"Bhushan Kathuria, M. Pareek, S. Kadam, Rigved nitala","doi":"10.5530/OGH.2017.6.1.4","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.1.4","url":null,"abstract":"","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"29 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129004815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Metastatic Insulinoma: Management and Review of Literature 转移性胰岛素瘤1例:治疗及文献复习
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-07-01 DOI: 10.5530/OGH.2016.5.2.10
A. Dubey, S. Viswanath
{"title":"A Case of Metastatic Insulinoma: Management and Review of Literature","authors":"A. Dubey, S. Viswanath","doi":"10.5530/OGH.2016.5.2.10","DOIUrl":"https://doi.org/10.5530/OGH.2016.5.2.10","url":null,"abstract":"How to cite this article: Dubey AP, Viswanath S. A case of metastatic insulinoma: Management and review of literature. OGH Reports, 2016; 5(2):79-81. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. A case of metastatic insulinoma: Management and review of literature","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"61 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128202091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
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