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Endoscopic Management of Bilio-Pleural Fistula following Thoracoabdominal Trauma 胸腹外伤后胆-胸膜瘘的内镜治疗
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2018-04-10 DOI: 10.5530/OGH.2018.7.1.14
T. Nikumbh, P. Barot, U. Kurlekar, A. Bapaye
{"title":"Endoscopic Management of Bilio-Pleural Fistula following Thoracoabdominal Trauma","authors":"T. Nikumbh, P. Barot, U. Kurlekar, A. Bapaye","doi":"10.5530/OGH.2018.7.1.14","DOIUrl":"https://doi.org/10.5530/OGH.2018.7.1.14","url":null,"abstract":"Copyright © 2018 Phcog.Net. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license. Cite this article: Nikumbh TN, Barot PV, Kurlekar UV, Bapaye AM. Endoscopic Management of Bilio-Pleural Fistula following Thoracoabdominal Trauma. OGH Reports. 2018;7(1):67-9. ABSTRACT Penetrating thoracoabdominal trauma, with potential injury to two anatomic cavities, poses a significant diagnostic and therapeutic challenge. This is especially true with reference to detection of diaphragmatic injuries, where development of a bilio-pleural fistula is a rare phenomenon. The optimal management in such cases has not been clearly defined as both conservative and emergency surgical approaches have been tried in acute settings. We report a patient who suffered an accidental penetrating wound to the right thoracoabdominal region. The patient developed a bilio-pleural fistula immediately following the injury with imaging showing an intact diaphragm. The case was managed conservatively using endoscopy as the primary modality for treating the primary condition as well as a rare complication of biliary stent migration. Thus an endoscopic approach is feasible in management of bilio-pleural fistula when used in properly selected cases.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"72 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125758450","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
Primary Cutaneous Anaplastic Large Cell Lymphoma – A Usual Malignancy with Unusual Presentation at an Uncommon Site: A Case Report 原发性皮肤间变性大细胞淋巴瘤——一种不寻常部位、不寻常表现的常见恶性肿瘤:1例报告
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2018-04-10 DOI: 10.5530/OGH.2018.7.1.12
G. Singh, Pragya Singh, P. B. Shanmuga, K. Periasamy, K. Bhowmik
{"title":"Primary Cutaneous Anaplastic Large Cell Lymphoma – A Usual Malignancy with Unusual Presentation at an Uncommon Site: A Case Report","authors":"G. Singh, Pragya Singh, P. B. Shanmuga, K. Periasamy, K. Bhowmik","doi":"10.5530/OGH.2018.7.1.12","DOIUrl":"https://doi.org/10.5530/OGH.2018.7.1.12","url":null,"abstract":"Copyright © 2018 Phcog.Net. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license. Cite this article: Singh GK, Singh P, Shanmuga PB, Periasamy K, Bhowmik KT. Primary cutaneous anaplastic large cell lymphoma – A usual malignancy with unusual presentation at an uncommon site: A case report. OGH Reports. 2018;7(1):53-5. ABSTRACT Malignant tumors of anal margin and perianal skin are rare, which accounts for approximately 2%-3% of all anorectal malignancies. Because of the variable presentation and pathologic similarity to benign anal lesions, the diagnosis and treatment is often delayed. We report the case of a 54-year-old Indian male who presented with non-healing anal fistula which progressed to a large chronic ulcer and was later diagnosed as anaplastic large cell lymphoma of perianal skin. Primary cutaneous anaplastic large cell lymphoma (PCALCL) of perianal area has been rarely reported, that too masquerading anal fistula is being reported for the first time.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"55 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117298724","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
First Report of Balloon-Occluded Antegrade Cyanoacrylate Glue Embolization (BAGE) for Bleeding Rectal Varices from India 来自印度的经球囊阻塞的顺行氰基丙烯酸酯胶栓塞治疗直肠静脉曲张出血的首例报道
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2018-04-10 DOI: 10.5530/OGH.2018.7.1.10
L. Kumar, C. Philips, P. Augustine
{"title":"First Report of Balloon-Occluded Antegrade Cyanoacrylate Glue Embolization (BAGE) for Bleeding Rectal Varices from India","authors":"L. Kumar, C. Philips, P. Augustine","doi":"10.5530/OGH.2018.7.1.10","DOIUrl":"https://doi.org/10.5530/OGH.2018.7.1.10","url":null,"abstract":"Copyright © 2018 Phcog.Net. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license. Cite this article: Kumar L, Philips CA, Augustine P. First Report of Balloon-Occluded Antegrade Cyanoacrylate Glue Embolization (BAGE) for Bleeding Rectal Varices from India. OGH Reports. 2018;7(1):46-8. ABSTRACT Rectal variceal bleeding occurs in 38% of patients with portal hypertension leading to an overall mortality in 5%. Conventional management involves endoscopic measures utilizing sclerotherapy/glue injection/banding ligation or surgical management. Some patients, mostly Child A or B cirrhotics, pose difficulty for traditional management and have been shown to benefit from transjugular intrahepatic portosystemic shunting (TIPSS) or interventional balloon occluded shunt embolization procedures, balloon occluded transvenous obliteration being the most common used modality, however, seldom reported in literature. In this report, we present the case, through striking images and real time step by step procedural video; of a difficult to control rectal variceal bleeding in a Child C cirrhotic in whom, balloon occluded antegrade glue embolization of multiple shunts was performed with beneficial outcomes.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"33 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"130337043","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
An Update on Infection and Cancer 感染与癌症的最新进展
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2018-04-10 DOI: 10.5530/OGH.2018.7.1.2
Sumeet Jain, Debasish Mohapatra, S. Satpathi, S. Senapati
{"title":"An Update on Infection and Cancer","authors":"Sumeet Jain, Debasish Mohapatra, S. Satpathi, S. Senapati","doi":"10.5530/OGH.2018.7.1.2","DOIUrl":"https://doi.org/10.5530/OGH.2018.7.1.2","url":null,"abstract":"","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"35 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127907929","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
Spontaneous perforation of GIST of the Small Intestine: A Rare Cause of Perforation Peritonitis 小肠间质间质自发性穿孔:穿孔性腹膜炎的罕见病因
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/OGH.2017.6.2.16
A. Saharan, S. Dalal, Mahavir Singh, Chisel Bhatia, R. Sen
{"title":"Spontaneous perforation of GIST of the Small Intestine: A Rare Cause of Perforation Peritonitis","authors":"A. Saharan, S. Dalal, Mahavir Singh, Chisel Bhatia, R. Sen","doi":"10.5530/OGH.2017.6.2.16","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.2.16","url":null,"abstract":"Gastrointestinal stromal tumors (GIST) are relatively rare and often present with vague symptoms. Their first clinical manifestation as acute abdomen due to perforation is extremely rare. We report a rare case of spontaneous perforation of exophytic gastrointestinal stromal tumor (GIST) causing perforation of jejunum. A 61 year, male patient presented with symptoms of acute abdomen. After evaluation, a laparotomy was performed, where perforation of a tumor in the jejunum was found. The perforated part along with the tumor was resected and the histopathological examination showed that the tumor was GIST. In emergency setting the patients with perforation peritonitis, a diagnosis of spontaneous perforation of GIST though rare should be kept in mind specially in elderly patients.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"63 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126316930","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
Primary Plasmacytoma of Thyroid Gland—an Interesting Case Diagnosed By FNAC 原发性甲状腺浆细胞瘤——一个有趣的FNAC诊断病例
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/OGH.2017.6.2.24
Debashish Bhattacharjee, S. Mondal, Goutam Dey, S. Biswas
{"title":"Primary Plasmacytoma of Thyroid Gland—an Interesting Case Diagnosed By FNAC","authors":"Debashish Bhattacharjee, S. Mondal, Goutam Dey, S. Biswas","doi":"10.5530/OGH.2017.6.2.24","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.2.24","url":null,"abstract":"Introduction: Primary plasmacytoma of the thyroid gland is a rare disease. Extramedullary plasmacytoma (EMP) comprises 3-5% of all plasma cell neoplasm. Case report: A 57-yearsold female presented with a large thyroid swelling involving the left lobe and isthmus, firm in consistency and moved a little with deglutition. CT scan revealed a large solid tumor (9.5 cm in greatest dimension) affecting thyroid gland. CT scan report gave differential diagnoses of plasmacytoma and metastatic carcinoma. FNAC revealed hypercellular smears composed of plasma cells with eccentrically placed nuclei and perinuclear hoff. Hematological work up and other relevant investigations including urine for Bence Jones protein ruled out multiple myeloma or other plasma cell dyscrasias. Subsequent histopathological examination and IHC (immunohistochemistry) confirmed the diagnosis of primary plasmacytoma of thyroid. Discussion: EMP can present with elevated anti thyroid antibodies and can be associated with lymphocytic thyroiditis; however, in our patient these findings were not present.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115198598","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
KAI-1 ad p53 expression in Odontogenic cysts: An Immuno-histochemical Marker Study 牙源性囊肿中KAI-1和p53的表达:免疫组织化学标志物研究
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/ogh.2017.6.2.14
A. Nayyar, N. Patil, M. Chaudhary, V. Wadhwan
{"title":"KAI-1 ad p53 expression in Odontogenic cysts: An Immuno-histochemical Marker Study","authors":"A. Nayyar, N. Patil, M. Chaudhary, V. Wadhwan","doi":"10.5530/ogh.2017.6.2.14","DOIUrl":"https://doi.org/10.5530/ogh.2017.6.2.14","url":null,"abstract":"","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"36 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123185455","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 Rare Case of Synovial Sarcoma Presenting in Paraspinal Region 少见的滑膜肉瘤出现在椎旁区
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/OGH.2017.6.2.25
Kaalindi Singh, P. Thakur, Mukesh K. Sharma
{"title":"A Rare Case of Synovial Sarcoma Presenting in Paraspinal Region","authors":"Kaalindi Singh, P. Thakur, Mukesh K. Sharma","doi":"10.5530/OGH.2017.6.2.25","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.2.25","url":null,"abstract":"Synovial sarcoma is an aggressive malignant neoplasm arising from mesenchymal tissue representing 7-10% of all soft tissue sarcomas. Typically, it presents in children and young adults aged 13-35 years of age. These are usually located in the extremities, most commonly around the knee. Paraspinal region is a rare site of synovial sarcoma and thus requires a high index of suspicion for timely diagnosis. Here, we discuss such a rare case of paraspinal synovial sarcoma.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132448036","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
Acute Promyelocytic Leukaemia(APML) in an Adult Patient Presenting with Multiple Lytic Bony Lesions – The First of its Kind – A Case Report with Review of Literature 急性早幼粒细胞白血病(APML)在成人患者中表现为多发性溶解性骨病变-首次此类-病例报告并文献复习
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/ogh.2017.6.2.23
Rajeev Lakkavalli Krishnappa, G. Kanakasetty, Suresh Babu Mallekavu Chikkadasappa, S. Rao
{"title":"Acute Promyelocytic Leukaemia(APML) in an Adult Patient Presenting with Multiple Lytic Bony Lesions – The First of its Kind – A Case Report with Review of Literature","authors":"Rajeev Lakkavalli Krishnappa, G. Kanakasetty, Suresh Babu Mallekavu Chikkadasappa, S. Rao","doi":"10.5530/ogh.2017.6.2.23","DOIUrl":"https://doi.org/10.5530/ogh.2017.6.2.23","url":null,"abstract":"Acute promyelocytic leukaemia presenting with bony lesions alongside medullary involvement is rare with anecdotal reports having noted this manifestation in a newly diagnosed case. We here report an infrequent presentation of a young adult male presenting solely with multiple axial and pelvic bone lesions initially, with the initial impression being a lymphoma /infiltrative lesion. This is a case report that reiterates the need for prompt diagnosis and a thorough evaluation for early treatment, especially since this is a curable malignancy.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"30 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117250946","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
Mass in the Adrenal Region: Not Always of Adrenal Origin: A Diagnostic Dilemma 肾上腺区肿块:不总是肾上腺起源:诊断困境
Oncology, Gastroenterology and Hepatology Reports Pub Date : 2017-03-01 DOI: 10.5530/OGH.2017.6.2.20
Suvendu Maji, M. Saha, S. Sahu
{"title":"Mass in the Adrenal Region: Not Always of Adrenal Origin: A Diagnostic Dilemma","authors":"Suvendu Maji, M. Saha, S. Sahu","doi":"10.5530/OGH.2017.6.2.20","DOIUrl":"https://doi.org/10.5530/OGH.2017.6.2.20","url":null,"abstract":"The rising incidence of incidentally detected adrenal masses reflects the ever growing use of radiologic investigations specially CT scans and MRI. The differential diagnosis is a long list which includes adenoma, myelolipoma, cyst, lipoma, pheochromocytoma, adrenal cancer, metastatic cancer, hyperplasia, and tuberculosis.[5] However rarely a schwannoma is considered in the list of provisional diagnosis. CT scan is often the first line of investigation of choice which along with endocrinological workup can point towards diagnosis. But none of them are 100% specific. Since the posterior mediastinum is anatomically in proximity to the adrenal area, a tumour in such a region can mimic an adrenal mass as was in our case. We herein report such an unusual case where a posterior mediastinal mass was found intraoperatively instead of a ‘presumed’ adrenal mass as suggested by preoperative radiological investigations!","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"15 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127636489","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
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