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遗传性血色素沉着症中的踝关节和后足关节病

Ankle and hindfoot arthropathy in hereditary hemochromatosis.

作者信息

Schmid Holger, Struppler Christiane, Braun Gerald S, Kellner Wolfgang, Kellner Herbert

机构信息

Rheumahaeinheit, Med. Poliklinik, Munich, Germany.

出版信息

J Rheumatol. 2003 Jan;30(1):196-9.

Abstract

Arthropathy is a leading clinical manifestation of hereditary hemochromatosis (HH), but involvement of the ankle and hindfoot joints is rare. We describe 3 male patients who presented with symmetrical pain and swelling of the ankles. Radiographs and magnetic resonance imaging showed severe osteoarthritic degenerative changes with a radiological triad of joint space narrowing, subchondral sclerosis, and cyst formation. In all 3 cases a homozygous C282Y mutation in the HFE gene was detected and liver biopsies confirmed the diagnosis of HH. Other differential diagnoses could be excluded. Severe arthropathy of the ankle and hindfoot in comparatively young men can be a leading presentation of HH.

摘要

关节病是遗传性血色素沉着症(HH)的主要临床表现,但踝关节和后足关节受累情况罕见。我们描述了3例男性患者,他们均出现踝关节对称性疼痛和肿胀。X线片和磁共振成像显示严重的骨关节炎退行性改变,伴有关节间隙变窄、软骨下硬化和囊肿形成的影像学三联征。所有3例均检测到HFE基因纯合C282Y突变,肝脏活检确诊为HH。其他鉴别诊断可以排除。相对年轻男性的严重踝关节和后足关节病可能是HH的主要表现。

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