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原发性食管黏膜相关淋巴组织淋巴瘤,表现为黏膜下肿瘤。

Primary mucosa-associated lymphoid tissue lymphoma of the esophagus, manifesting as a submucosal tumor.

作者信息

Jung Jae Gu, Kang Hyoun Woo, Hahn Suk Jae, Choi Jong Sun, Kim Eung Joong

机构信息

Department of Internal Medicine, Dongguk University Ilsan Hospital, 27 Donggung-ro, Ilsandong-gu, Goyang 410-773, Korea.

出版信息

Korean J Gastroenterol. 2013 Aug 25;62(2):117-21. doi: 10.4166/kjg.2013.62.2.117.

Abstract

We report a case of primary mucosa-associated lymphoid tissue (MALT) lymphoma in the esophagus that manifested as a large submucosal tumor (SMT). Primary esophageal lymphoma is very rare, occurring in less than 1% of all patients with gastrointestinal lymphoma. Only a few cases of MALT lymphoma in the esophagus have been reported in the English literature. A 53-year-old man was referred to Dongguk University Ilsan Hospital (Goyang, Korea) in July 2012 for further evaluation and treatment of an esophageal SMT. Endoscopy showed a cylindrically elongated submucosal mass with normal overlying mucosa in the mid esophagus, 25-30 cm from the incisor teeth. He underwent surgery to confirm the diagnosis. Pathologic findings showed diffuse small atypical lymphoid cells which were stained with Bcl-2, CD20, but not with CD3, CD5, CD23, Bcl-6, or cyclin D1. These cells showed a positive monoclonal band for immunoglobulin heavy chain gene rearrangement. Based on the pathological, immunohistochemical, and molecular biological features, the esophageal mass was diagnosed as extranodal marginal zone B-cell lymphoma of the MALT type.

摘要

我们报告一例食管原发性黏膜相关淋巴组织(MALT)淋巴瘤,表现为巨大黏膜下肿瘤(SMT)。原发性食管淋巴瘤非常罕见,在所有胃肠道淋巴瘤患者中发生率不到1%。英文文献中仅报道了少数几例食管MALT淋巴瘤病例。一名53岁男性于2012年7月转诊至韩国高阳的东国大学一山医院,以进一步评估和治疗食管SMT。内镜检查显示,在距门齿25 - 30 cm的食管中段有一个圆柱形细长的黏膜下肿块,其上方黏膜正常。他接受了手术以明确诊断。病理结果显示弥漫性小的非典型淋巴细胞,这些细胞Bcl - 2、CD20染色阳性,但CD3、CD5、CD23、Bcl - 6或细胞周期蛋白D1染色阴性。这些细胞免疫球蛋白重链基因重排显示单克隆带阳性。根据病理、免疫组化和分子生物学特征,该食管肿块被诊断为MALT型结外边缘区B细胞淋巴瘤。

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