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Indolent Gastrointestinal Mantle Cell Lymphoma with Multiple Lymphomatous Polyposis, Report of a Case Takashi Murakami 1 , Takashi Yao 2 , Eiji Kamba 1 , Kei Nomura 1 , Keiichi Haga 1 , Hirofumi Fukushima 1 , Tomoyoshi Shibuya 1 , Akihito Nagahara 1 1Department of Gastroenterology, Juntendo University School of Medicine, Tokyo 2Department of Human Pathology, Juntendo University School of Medicine, Tokyo Keyword: マントル細胞リンパ腫 , MCL , 悪性リンパ腫 , 消化管悪性リンパ腫 , MLP , multiple lymphomatous polyposis , 免疫組織化学染色 pp.921-927
Published Date 2023/7/25
DOI https://doi.org/10.11477/mf.1403203277
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 A female patient in her 60s underwent a colonoscopy at a local clinic for fecal occult blood, which revealed clusters of lymphoid follicle-like granules in the terminal ileum. She was referred to our hospital for a detailed examination. A comprehensive endoscopic investigation revealed multiple lymphomatous polyposis with a smooth surface in the terminal ileum, the ileocecal valve, the sigmoid colon, and the rectum. A biopsy was performed. Histopathological assessment of the mucosa revealed densely packed small- to medium-sized atypical lymphocytes with constricted nuclei. Immunohistologically, CD20, CD5, Cyclin D1, and Bcl-2 were positive, whereas CD3 and CD10 were negative. She was diagnosed with MCL(mantle cell lymphoma). Positron emission tomography-computed tomography revealed terminal ileal wall thickening with weak FDG(18F-fluorodeoxyglucose)accumulation and bilateral cervical, left axillary, and bilateral inguinal lymph node enlargement, all with FDG accumulation. Bone marrow infiltration was not observed, and the Ki-67 positivity was low. Therefore, these lesions were suspected to be indolent MCL. The patient is currently being followed up and has been doing well.


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