Migueletto B C, Neto A E, Domingues E Z, Neves de Castro P P, Stocker H, Marie S K, Meireles L P, Arai M H
Department of Clinical Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.
Rev Hosp Clin Fac Med Sao Paulo. 1999 Sep-Oct;54(5):165-8. doi: 10.1590/s0041-87811999000500007.
Primary biliary cirrhosis (PBC) is a cholestatic liver disease, which is characterized by a chronic inflammatory destruction of intrahepatic bile ducts. It is a rare disorder whose precise etiology is still to be elucidated. Even though the liver is the principal target of PBC, other organ systems also might be affected. Muscular involvement has rarely been described in this disease, and in the majority of cases, muscular weakness has been interpreted as polymyositis. We report the case of a 48-year-old woman suffering from classic PBC, in association with a myopathy whose histological features are distinct from the cases reported before. We also performed a MEDLINE research for PBC and concomitant muscular diseases.
原发性胆汁性肝硬化(PBC)是一种胆汁淤积性肝病,其特征是肝内胆管的慢性炎症性破坏。它是一种罕见的疾病,确切病因仍有待阐明。尽管肝脏是PBC的主要靶器官,但其他器官系统也可能受到影响。在这种疾病中,肌肉受累的情况很少被描述,在大多数病例中,肌无力被解释为多发性肌炎。我们报告了一例48岁患有典型PBC的女性病例,该病例伴有一种组织学特征与既往报道病例不同的肌病。我们还对PBC和伴发的肌肉疾病进行了医学文献联机数据库(MEDLINE)检索。