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A case of primary biliary cirrhosis complicated by Behçet’s disease and palmoplantar pustulosis

机译:一例原发性胆汁性肝硬化并发白塞氏病和掌plant脓疱病

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摘要

A 46-year-old woman was diagnosed with palmoplantar pustulosis (PPP) at the Department of Dermatology, Fukushima Medical University Hospital in 2000, and was treated with ointment. However, because liver dysfunction developed in 2003, she was referred to our department, where primary biliary cirrhosis (PBC) was also diagnosed on the basis of clinical findings. One year later, at the age of 49, she developed manifestations of Behçet’s disease (BD), including erythema nodosum in the lower extremities. Because she had a history of uveitis, recurrent oral ulceration was present, and the HLA typing was positive for B51, BD was additionally diagnosed. Liver function normalized within three months of the start of treatment with ursodesoxycholic acid (UDCA). This is the first case of PBC associated with BD and PPP.
机译:2000年,一名46岁的妇女在福岛医科大学附属医院皮肤科被确诊为掌plant脓疱病(PPP),并接受了软膏治疗。但是,由于肝功能障碍于2003年发展,她被转诊到我们的科室,​​在该科室还根据临床发现诊断出原发性胆汁性肝硬化(PBC)。一年后,在49岁的时候,她出现了Behçet病(BD)的表现,包括下肢的结节性红斑。因为她有葡萄膜炎病史,所以经常出现口腔溃疡,并且HLA分型为B51阳性,因此还诊断出BD。在用熊去氧胆酸(UDCA)治疗开始后的三个月内,肝功能恢复正常。这是与BD和PPP相关的PBC的第一种情况。

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