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抗线粒体抗体阴性的原发性胆汁性肝硬化

Antimitochondrial antibody-negative primary biliary cirrhosis.

作者信息

Mendes Flavia, Lindor Keith D

机构信息

Division of Hepatology, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

出版信息

Gastroenterol Clin North Am. 2008 Jun;37(2):479-84, viii. doi: 10.1016/j.gtc.2008.02.006.

Abstract

There is a subset of patients who have biochemical and histologic features consistent with primary biliary cirrhosis (PBC) who lack antimitochondrial antibodies (AMA). This entity is usually referred to as AMA-negative PBC or alternatively autoimmune cholangitis. Patients who have AMA-negative PBC are believed to have a similar clinical course, response to treatment, and prognosis as their AMA-positive counterparts. As more sensitive and specific serologic tests are developed to detect serum AMA, it is possible we may find that these patients initially believed to be AMA-negative are indeed AMA-positive, suggesting a single disease process.

摘要

有一部分患者具有与原发性胆汁性肝硬化(PBC)相符的生化和组织学特征,但缺乏抗线粒体抗体(AMA)。这种情况通常被称为AMA阴性PBC,或者称为自身免疫性胆管炎。AMA阴性PBC患者被认为与AMA阳性患者具有相似的临床病程、对治疗的反应和预后。随着用于检测血清AMA的更敏感和特异的血清学检测方法的开发,有可能我们会发现这些最初被认为是AMA阴性的患者实际上是AMA阳性,这表明是单一的疾病过程。

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