Kadayifçi A, Benekli M, Savaş M C, Arslan S, Uzunalimoğlu B, Barişta I, Güllü I H, Tekuzman G
Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Turkey.
J Surg Oncol. 1997 Apr;64(4):336-40. doi: 10.1002/(sici)1096-9098(199704)64:4<336::aid-jso16>3.0.co;2-0.
Multiple lymphomatous polyposis (MLP) is a distinctive and particularly rare clinical type of malignant gastrointestinal lymphoma, which is classified as B-cell centrocytic non-Hodgkin's lymphoma. this rare entity has been recently reclassified as mantle cell lymphoma. We herein report three additional cases of MLP involving various segments of the gastrointestinal tract. MLP has an aggressive biologic behavior and a relatively poor prognosis and must be treated accordingly as a high-grade lymphoma with systemic chemotherapy.
多发性淋巴瘤性息肉病(MLP)是一种独特且极为罕见的恶性胃肠道淋巴瘤临床类型,被归类为B细胞中心细胞型非霍奇金淋巴瘤。这种罕见的实体最近已重新归类为套细胞淋巴瘤。我们在此报告另外3例累及胃肠道不同节段的MLP病例。MLP具有侵袭性生物学行为且预后相对较差,必须作为高级别淋巴瘤采用全身化疗进行相应治疗。