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CyclinD1阴性的消化道套细胞淋巴瘤1例

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摘要 套细胞淋巴瘤(Mantle cell lymphoma,MCL)是一种小B细胞非霍奇金淋巴瘤,因其肿瘤细胞在淋巴节内呈套区生长模式及伴有染色体t(11;14)(q13;q32)异常而被世界卫生组织(WHO)造血与淋巴组织分类归为一种独立的疾病。MCL发病率占非霍奇金淋巴瘤(non-Hodgkin lymphoma,NHL)的6%,北美年发病率1/10万[1],西欧年发病率(1-2)/10万[2]。大部分MCL的临床表现早期多不典型,患者确诊时多已呈弥散性病变,处于Ⅲ-Ⅳ期。淋巴结多受累,其次是胃肠道,在消化道主要表现为淋巴瘤样息肉,并出现与之相关的胃肠道出血及腹痛症状。临床诊治过程中极易误诊为肠息肉病,目前国内对MCL的研究较少,现将北京市普仁医院收治的1例首诊于消化科的MCL病例报告如下。
出处 《山西医科大学学报》 CAS 2019年第6期860-862,共3页 Journal of Shanxi Medical University
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