Brzezińska-Kolarz B, Undas A, Dyczek A, Musiał J
II Katedra Chorób Wewnetrznych Collegium Medicum Uniwersytetu Jagiellońskiego w Krakowie.
Pol Arch Med Wewn. 2001 Mar;105(3):231-4.
A 57-year--woman with Reynolds syndrome (primary biliary cirrhosis and scleroderma) is reported. Diagnosis of primary biliary cirrhosis is based on clinical findings, laboratory tests results and histological result of liver biopsy. Scleroderma was confirmed by anticentromere antibodies presence, and typical skin lesions. Although, antimitochondrial antibodies are very typical for PBC (primary biliary cirrhosis), in this case the were not found.
报道了一名患有雷诺氏综合征(原发性胆汁性肝硬化和硬皮病)的57岁女性。原发性胆汁性肝硬化的诊断基于临床症状、实验室检查结果以及肝脏活检的组织学结果。硬皮病通过抗着丝点抗体的存在以及典型的皮肤病变得以确诊。尽管抗线粒体抗体对原发性胆汁性肝硬化非常典型,但在该病例中未检测到。