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A rare case of mantle cell lymphoma as lymphomatous polyposis with widespread involvement of the digestive tract.

机译:罕见的套细胞淋巴瘤为淋巴瘤性息肉病,广泛累及消化道。

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摘要

Lymphomatous polyposis of the gastrointestinal tract is rare. It refers to a heterogeneous group of small B-cell lymphomas including mantle cell lymphoma, follicular lymphoma and MALT lymphoma. It is characterized by the presence of multiple lymphomatous polyps along one or more segments of the digestive tract. Clinical symptoms are non-specific. We herein report the case of a 74-year old man initially admitted for an upper and lower gastrointestinal endoscopy to explore a positive Hemoccult test. The endoscopy revealed multiple polyps all along the gastrointestinal tract. Histopathological study showed a diffuse lymphomatous proliferation of small B-cells whose immunohistochemical features were compatible with a mantle cell lymphoma. Tumoral B-cells showed a positivity of cyclin D1 markers but negativity for CD5. Immunochemotherapy with R-CHOP (rituximab, cyclophosphamide, adriamycine, vincristine and prednisone) was initiated. Based on this case study, the pitfalls of gastrointestinal tract lymphomatous polyposis diagnosis, prognosis and treatment options are discussed.
机译:胃肠道淋巴瘤性息肉病很少见。它是指一组异质性小B细胞淋巴瘤,包括套细胞淋巴瘤,滤泡性淋巴瘤和MALT淋巴瘤。其特征是沿消化道的一个或多个节段存在多个淋巴瘤性息肉。临床症状是非特异性的。我们在此报告了一名74岁的男性患者,该患者最初被接受上消化道和下消化道内镜检查,以探索阳性的血液学检查。内窥镜检查显示整个胃肠道内有多个息肉。组织病理学研究显示小B细胞的弥漫性淋巴瘤增殖,其免疫组织化学特征与套细胞淋巴瘤相容。肿瘤B细胞显示细胞周期蛋白D1标记阳性,但CD5阴性。开始使用R-CHOP(利妥昔单抗,环磷酰胺,阿霉素,长春新碱和泼尼松)进行免疫化学疗法。在此案例研究的基础上,讨论了胃肠道淋巴瘤性息肉病的陷阱,诊断,预后和治疗方案。

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