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[原发性肠道T细胞淋巴瘤伴大量嗜酸性粒细胞增多症]

[Primary intestinal T lymphoma with massive eosinophilia].

作者信息

Remacha Tomey B, Colom J, Ripollés V, Cortés Vizcaíno V, Vera Román J

机构信息

Sección de Aparato Digestivo, Hospital General de Castellón.

出版信息

Gastroenterol Hepatol. 1999 Feb;22(2):82-5.

Abstract

Primary intestinal T lymphoma with eosinophilia is an infrequent tumour. Its rarity account for the paucity of similar cases recorded in the literature. It affects predominantly middle-aged men and may be associated with ulceration, fistula formation and intestinal perforation with an abdominal mass. Lesions of the intestine with massive tissue eosinophilia may be a difficult diagnostic problem, but this entity displays distinctive histological features. The presence of intense tissue eosinophilia is a T-cell dependent lymphomas response. We describe a case of T lymphoma involving small intestine with massive eosinophilia.

摘要

原发性肠道嗜酸性粒细胞增多性T淋巴瘤是一种罕见的肿瘤。其罕见性导致文献中记录的类似病例较少。它主要影响中年男性,可能与溃疡、瘘管形成以及伴有腹部肿块的肠穿孔有关。伴有大量组织嗜酸性粒细胞增多的肠道病变可能是一个诊断难题,但该实体具有独特的组织学特征。强烈的组织嗜酸性粒细胞增多是一种T细胞依赖性淋巴瘤反应。我们描述了一例累及小肠并伴有大量嗜酸性粒细胞增多的T淋巴瘤病例。

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