原发性胆汁性肝硬化与抗磷脂综合征相关。

Israel journal of medical sciences Pub Date : 1997-10-01
M Hoffman, M Burke, M Fried, D Turner, Y Yosipov, I Yust
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引用次数: 0

摘要

患者47岁,女性,因右脚第三和第四趾剧烈疼痛1个月而入院,最终导致坏疽。实验室结果显示肝酶异常,抗线粒体、抗磷脂、抗核和可疑的抗dna抗体。系统性红斑狼疮(SLE)在6年随访后排除临床理由。因此,诊断为原发性抗磷脂综合征,并发微血管病变,并与原发性胆汁性肝硬化相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary biliary cirrhosis associated with antiphospholipid syndrome.

A 47-year-old female was admitted for severe pain of 1 month's duration in the third and fourth toes of the right foot, culminating in gangrene. Laboratory findings revealed liver enzyme abnormalities, and anti-mitochondrial, anti-phospholipid and antinuclear and doubtful anti-DNA antibodies. Systemic lupus erythematosus (SLE) was excluded on clinical grounds after a 6-year follow-up. Therefore, a diagnosis was made of the primary antiphospholipid syndrome, complicated by microvasculopathy, and associated with primary biliary cirrhosis.

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