V. Rana, Ranjan Praveer, Singh Giriraj, Rathi Khushi Ram
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.
{"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}
Suresh Babu Mallekavu Chikkadasappa, G. Kanakasetty, Rajeev Lakkavalli Krishnappa, S. Rao
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.
{"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}
{"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}
Sonal Saran, P. Khera, R. Rajagopal, Neeraj Mehta, P. Elhence
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.
{"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}
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.
{"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}
M. Rasool, Najmi Arshad Manzoor, Shareefa Akhter, Bhat Altaf Rasool, S. A. Bashir
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.
{"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}
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.
国际许可。本文引自:Bansal M, Gupta R, Bansal J.腹腔疾病:世界出版物数量的科学计量分析，2005-2014。健康报告，2017;6(1):8-15。摘要本文分析了Scopus数据库2005- 2014年14317篇关于乳糜泻的论文，平均年增长率为5.20%，引用影响为12.53。在2005- 2014年期间，15个生产力最高的国家占世界产出的83.89%，其中最大的份额(21.40%)来自美国，其次是意大利(12.61%)、英国(8.23%)、德国(5.41%)等。美国占全球引用份额的35.13%，其次是意大利(17.16%)、英国(15.74%)等。发表率最高的是医学(87.93%)，其次是生物化学、遗传学与分子生物学(13.56%)、免疫学与微生物学(6.73%)、农业与生物科学(5.57%)、护理学(3.07%)、药理学、毒理学与药剂学(2.74%)、神经科学(2.26%)等。2005- 2014年期间，按症状分类的出版物中，腹泻所占比例最大(8.10%)，其次是腹痛(7.68%)、胰岛素依赖型糖尿病(6.84%)、克罗恩病(6.22%)、肠炎(5.34%)等。在显著关键词中，无麸质饮食所占比例最大(18.47%)。在2005-14年期间，15个生产力最高的组织、作者和期刊分别占世界出版产出的15.06%、10.71%和16.57%。结论是，各国必须促进全球研究与发展，增加对研究与开发的投资，增加其专业人力，并向科学家和研究人员提供适当的培训课程和基础设施，以控制这种疾病蔓延所面临的挑战。
{"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}
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.
{"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}
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}
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
Dubey AP, Viswanath S. 1例转移性胰岛素瘤的治疗和文献复习。OGH报告，2016;5(2): 79 - 81。这是一篇在知识共享署名-非商业-相同方式共享3.0许可条款下发布的开放获取文章，该许可允许其他人在作者署名和新创作在相同条款下授权的情况下，以非商业方式重新混合、调整和构建作品。转移性胰岛素瘤1例:治疗及文献复习
{"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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：