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一例形成肿块的结肠原发性套细胞淋巴瘤。

A Single Mass Forming Colonic Primary Mantle Cell Lymphoma.

作者信息

Daniel Fady, Assi Hazem I, Karaoui Walid, El Cheikh Jean, Bannoura Sami, Nassif Samer

机构信息

Division of Gastroenterology, Department of Internal Medicine, American University of Beirut Medical Center, P.O. Box 11-0236, Riad El Solh, Beirut 110-72020, Lebanon.

Division of Hematology & Oncology, Department of Internal Medicine, American University of Beirut Medical Center, P.O. Box 11-0236, Riad El Solh, Beirut 110-72020, Lebanon.

出版信息

Case Rep Gastrointest Med. 2016;2016:2561507. doi: 10.1155/2016/2561507. Epub 2016 Aug 4.

Abstract

Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin's lymphoma (NHL) comprising around 7% of adult NHL. It is characterized by a chromosomal translocation t(11:14) and overexpression of Cyclin D1. The incidence of secondary gastrointestinal tract involvement in MCL ranges from 10 to 28% in various series. However primary gastrointestinal MCL is very rare, accounting for only 1 to 4% of primary gastrointestinal lymphomas. The most common endoscopic feature of primary intestinal MCL is multiple lymphomatous polyposis. In rare cases it presents as protruded lesions or superficial lesions. Single colonic mass presentation is an extremely infrequent presentation. MCL has an aggressive course with quick progression, and most cases are discovered in the advanced stages. Colonic biopsies with histologic examination and specific immunohistochemical staining are the gold standard for a proper diagnosis. We report a case of a single mass forming mantle cell lymphoma of the ascending colon in a 57-year-old female patient with unusual colonoscopic and radiologic features and describe the therapy the patient received, thereby adding to the spectrum of clinical presentations of this aggressive lymphoproliferative disorder.

摘要

套细胞淋巴瘤(MCL)是非霍奇金淋巴瘤(NHL)的一种亚型,约占成人NHL的7%。其特征为染色体易位t(11;14)及细胞周期蛋白D1过表达。在不同系列研究中,MCL继发胃肠道受累的发生率为10%至28%。然而,原发性胃肠道MCL非常罕见,仅占原发性胃肠道淋巴瘤的1%至4%。原发性肠道MCL最常见的内镜特征是多发性淋巴瘤性息肉病。在罕见情况下,它表现为突出性病变或浅表性病变。单个结肠肿块表现极为罕见。MCL病程侵袭性强、进展迅速,大多数病例在晚期才被发现。结肠活检进行组织学检查及特异性免疫组化染色是正确诊断的金标准。我们报告一例57岁女性患者升结肠单发肿块型套细胞淋巴瘤,其具有不寻常的结肠镜和放射学特征,并描述了该患者接受的治疗,从而丰富了这种侵袭性淋巴增殖性疾病的临床表现谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a79/4989071/1c569433724a/CRIGM2016-2561507.001.jpg

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