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胶原性肠病与 HFE 血色病同时发生。

Concomitant presentation of collagenous sprue and HFE hemochromatosis.

机构信息

The Cleveland Clinic, Department of Gastroenterology and Hepatology, USA.

出版信息

J Crohns Colitis. 2011 Aug;5(4):369-72. doi: 10.1016/j.crohns.2011.03.009. Epub 2011 Apr 29.

Abstract

Collagenous sprue (CS) is a progressive malabsorptive disorder characterized by collagen deposition beneath the basement membrane of small bowel epithelium in refractory celiac sprue. CS is a pathologically distinct entity from celiac disease, despite a similar clinical presentation. The etiology of CS is unclear, although there are speculations that CS and celiac disease may share similar pathogenetic pathways. On the other hand, HFE hemochromatosis (HH) is a distinct disease entity. Celiac disease and HH are common HLA-associated genetic disorders in Northern European populations. There are a few case reports linking celiac disease and HH. We present a patient diagnosed with concurrent CS and HH.

摘要

胶原性肠病(CS)是一种进行性吸收不良疾病,其特征是在难治性乳糜泻的小肠上皮基底膜下有胶原沉积。CS 是一种与乳糜泻在病理上明显不同的实体,尽管临床表现相似。CS 的病因尚不清楚,尽管有推测认为 CS 和乳糜泻可能有相似的发病途径。另一方面,遗传性血色病(HH)是一种明确的疾病实体。乳糜泻和 HH 是北欧人群中常见的与 HLA 相关的遗传疾病。有一些病例报告将乳糜泻和 HH 联系起来。我们报告了一例同时诊断为 CS 和 HH 的患者。

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