R. Sareen, Menka Kapil, G. Gupta, D. Agrawal
{"title":"Rare Incidental Occurrence of Mantle Cell Lymphoma with Alcoholic Liver Disease and Pancreatitis","authors":"R. Sareen, Menka Kapil, G. Gupta, D. Agrawal","doi":"10.5530/ogh.2018.7.1.11","DOIUrl":null,"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: Sareen R, Kapil M, Gupta GN, Agrawal D. Rare Incidental Occurrence of Mantle Cell Lymphoma with Alcoholic Liver Disease and Pancreatitis. OGH Reports. 2018;7(1):49-52. ABSTRACT We present an extremely rare case of Mantle cell Lymphoma with concomitant alcoholic liver disease and pancreatitis in a 48 year old male patient. There was absence of abdominal lymphadenopathy. The complete blood count showed absolute lymphocytosis which on subsequent peripheral blood examination showed small to medium sized atypical cells raising suspicion of prolymphocytic leukemia. The flow cytometry and Immunohistochemistry examination confirmed Mantle cell lymphoma. The morphology of cells in mantle cell lymphoma are known to mimic prolymphocytes on peripheral blood. However, the rare concomitant occurrence of both diseases makes the case an interesting one for readers and emphasizes on the usefulness of peripheral blood examination although not completely diagnostic but raising an alarm for the diagnosis of this rare lymphoma.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology, Gastroenterology and Hepatology Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/ogh.2018.7.1.11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
套细胞淋巴瘤合并酒精性肝病和胰腺炎的罕见偶发
版权所有©2018phcog.net这是一篇基于知识共享署名4.0国际许可协议的开放获取文章。本文引用:Sareen R, Kapil M, Gupta GN, Agrawal D.少见的酒精性肝病和胰腺炎附带套细胞淋巴瘤。健康报告,2018;7(1):49-52。我们报告一例极为罕见的套细胞淋巴瘤合并酒精性肝病和胰腺炎的病例,患者为48岁男性。未见腹部淋巴结病。全血细胞计数显示绝对淋巴细胞增多,随后的外周血检查显示小到中等大小的非典型细胞,怀疑是前淋巴细胞白血病。流式细胞术及免疫组化检查证实为套细胞淋巴瘤。已知套细胞淋巴瘤的细胞形态类似于外周血中的前淋巴细胞。然而,这两种疾病罕见的同时发生,使得这个病例对读者来说是一个有趣的病例,并强调外周血检查的有用性,虽然不能完全诊断,但对这种罕见淋巴瘤的诊断提出了警告。
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