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结缔组织病与肝脏

Connective tissue diseases and the liver.

作者信息

Youssef Wael I, Tavill Anthony S

机构信息

Division of Gastroenterology and The Robert Schwartz Center for Metabolism and Nutrition at MetroHealth Medical Center, Case Western Reserve University, Cleveland, Ohio 44109, USA.

出版信息

J Clin Gastroenterol. 2002 Oct;35(4):345-9. doi: 10.1097/00004836-200210000-00012.

Abstract

Connective tissue diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis, Sjögren's syndrome, and scleroderma are systemic disorders that may have an autoimmune basis. The system manifestations vary, and there is frequent overlap among the syndromes. Liver involvement in patients with connective tissue diseases has been well documented but is generally considered rare. Although advanced liver disease with cirrhosis and liver failure is rare in patients with connective tissue diseases, clinical and biochemical evidence of associated liver abnormalities is common. Previous treatment with potentially hepatotoxic drugs or coincident viral hepatitis has usually been implicated as the main causes of liver disease in patients with connective tissue diseases. However, even after careful exclusion of these etiologies, the question remains whether to classify the patient as having a primary liver disease with associated autoimmune, clinical, and laboratory features or as having liver disease as a manifestation of generalized connective tissue disease. The main example of this pathogenetic dilemma is autoimmune hepatitis and SLE-associated hepatitis, which have been regarded as two different entities, although they have features in common of autoimmune syndromes. Several clinical and histopathologic features have been used to discriminate autoimmune hepatitis from SLE, a relevant diagnostic exercise because complications and therapy are quite different. Although hepatic steatosis and abnormal results on biochemical liver function tests are the most common hepatic abnormalities associated with connective tissue diseases, other less frequent abnormalities have been noted, such as nodular regenerative hyperplasia, portal vein obliteration and portal hypertension, features of primary biliary cirrhosis, and rarely portal fibrosis with abnormal lobular architecture. Vascular disorders of the liver also have been described, such as Budd-Chiari syndrome. Histologic assessment may reveal a variety of subclinical liver diseases. The aim of this contribution is to review the current published data regarding liver involvement in connective tissue diseases.

摘要

系统性红斑狼疮(SLE)、类风湿关节炎、干燥综合征和硬皮病等结缔组织病是可能具有自身免疫基础的全身性疾病。其系统表现各不相同,且各综合征之间常有重叠。结缔组织病患者肝脏受累已有充分记录,但一般认为较为罕见。尽管结缔组织病患者中晚期肝病伴肝硬化和肝衰竭很少见,但相关肝脏异常的临床和生化证据却很常见。既往使用潜在肝毒性药物治疗或合并病毒性肝炎通常被认为是结缔组织病患者肝病的主要原因。然而,即使仔细排除这些病因后,问题仍然存在,即该将患者归类为患有伴有自身免疫、临床和实验室特征的原发性肝病,还是将肝病归类为全身性结缔组织病的一种表现。这种发病机制困境的主要例子是自身免疫性肝炎和SLE相关肝炎,尽管它们具有自身免疫综合征的共同特征,但一直被视为两种不同的疾病。一些临床和组织病理学特征已被用于区分自身免疫性肝炎和SLE,这是一项相关的诊断工作,因为并发症和治疗方法有很大不同。尽管肝脂肪变性和生化肝功能检查结果异常是与结缔组织病相关的最常见肝脏异常,但也注意到了其他不太常见的异常,如结节性再生性增生、门静脉闭塞和门静脉高压、原发性胆汁性肝硬化的特征,以及罕见的伴有小叶结构异常的门静脉纤维化。肝脏血管疾病也有报道,如布加综合征。组织学评估可能揭示各种亚临床肝病。本文的目的是综述目前已发表的关于结缔组织病肝脏受累情况的数据。

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