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青少年男性以幼年特发性关节炎形式表现的厚皮性骨膜病。

Pachydermodactyly presenting as juvenile idiopathic arthritis in an adolescent man.

机构信息

University Hospitals of Leicester NHS Trust, Leicester, UK.

University Hospitals of Leicester NHS Trust, Leicester, UK

出版信息

BMJ Case Rep. 2021 Jan 18;14(1):e237214. doi: 10.1136/bcr-2020-237214.

Abstract

We present the case of a 17-year-old Asian man diagnosed with pachydermodactyly, a rare digital fibromatosis. Although this is a non-inflammatory periarticular soft tissue disorder, the clinical appearance can mimic inflammatory arthritis. The patient had a 2-year history of fusiform swelling of multiple proximal interphalangeal joints. He was initially diagnosed with juvenile idiopathic arthritis and treated with methotrexate, but a lack of clinical response led to the diagnosis of pachydermodactyly. Recognising this rare condition can prevent unnecessary and potentially harmful treatment.

摘要

我们报告了一例 17 岁亚洲男性患有厚皮性骨膜病的病例,这是一种罕见的手指纤维瘤病。尽管这是一种非炎症性的关节周围软组织疾病,但临床表现可能类似于炎症性关节炎。该患者有 2 年的多个近节指间关节梭形肿胀病史。他最初被诊断为幼年特发性关节炎,并接受了甲氨蝶呤治疗,但缺乏临床反应导致了厚皮性骨膜病的诊断。认识到这种罕见疾病可以避免不必要的和潜在有害的治疗。

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Pachydermodactyly: a review.厚皮性指节垫:综述
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Unusual unilateral presentation of pachydermodactyly: a case report.厚皮性骨膜病单侧表现异常:一例报告。
Rheumatol Int. 2012 Jun;32(6):1747-50. doi: 10.1007/s00296-011-1895-x. Epub 2011 Mar 26.
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