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[原发性肠道T细胞淋巴瘤:两例报告并文献复习]

[Primary intestinal T lymphoma: a report of two cases and a review of the literature].

作者信息

Molina Villaverde R, Jiménez Gordo A, López González J L, Redondo Sánchez A, Andreu Rodríguez M, González Barón M

机构信息

Servicio de Oncología Médica, Hospital La Paz, Paseo de la Castellana 261, 28046 Madrid.

出版信息

An Med Interna. 2002 Sep;19(9):457-9.

Abstract

Lymphomas of the gastrointestinal tract are the most common type of primary extranodal lymphomas and about 15-20% of these are primary intestinal lymphomas. They may be or B or T- cell. Intestinal T-cell lymphomas are much less common and they can be enteropathy-associated. This disease occurs in adults with abdominal pain often associated with intestinal perforation. The course is aggressive. The major problem is to distinguish this disease from a benign ulcer. Two cases with differents clinical and pathologic features are reported with a review in the literature of this uncommon entity.

摘要

胃肠道淋巴瘤是最常见的原发性结外淋巴瘤类型,其中约15%-20%为原发性肠道淋巴瘤。它们可以是B细胞或T细胞淋巴瘤。肠道T细胞淋巴瘤则少见得多,且可与肠病相关。这种疾病发生于成人,常伴有腹痛,且常与肠穿孔有关。病程进展迅速。主要问题是将这种疾病与良性溃疡区分开来。本文报告了两例具有不同临床和病理特征的病例,并对这一罕见实体的文献进行了综述。

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