免疫增生性小肠疾病1例报告及文献复习。

B W Trotman, A C Pavlick, I C Igwegbe, M M Goldstein
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引用次数: 0

摘要

免疫增生性小肠疾病(IPSID)是粘膜相关淋巴组织淋巴瘤的一种亚型。以α -重链的大量产生而著称,被称为α -重链病。IPSID是一种使人衰弱的疾病,多发于发展中国家的贫困人口。它主要在中东国家的受试者中被记录,因此以前被称为地中海淋巴瘤。我们报告一例来自塞内加尔的42岁男子,他表现为慢性腹泻、脱水和体重减轻。在用磷酸氟达拉滨治疗之前、期间和之后的内镜、病理和血清学检查结果被提出。我们回顾了目前关于IPSID的病因、发病机制和治疗的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoproliferative small intestinal disease: case report and literature review.

Immunoproliferative small intestinal disease (IPSID) is a subtype of lymphoma of mucosa-associated lymphoid tissue. Notable for a high production of alpha-heavy chains, it is designated alpha-heavy-chain disease. IPSID is a debilitating disease that has a predilection for impoverished populations of developing countries. It has been documented primarily in subjects of Middle Eastern countries and thus was previously referred to as Mediterranean lymphoma. We report the case of a 42-year-old man from Senegal who presented with chronic diarrhea, dehydration, and weight loss. The endoscopic, pathologic, and serologic findings before, during, and after treatment with fludarabine phosphate are presented. We review the literature concerning current concepts on the etiology, pathogenesis, and management of IPSID.

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