Faraawi R, Harth M, Kertesz A, Bell D
University Hospital, Department of Medicine, University of Western Ontario, London, Canada.
J Rheumatol. 1993 Mar;20(3):448-52.
We reviewed the clinical and radiographic features of arthropathy in 25 subjects with hemochromatosis, 16 probands and 9 discovered homozygous relatives. Clinical arthritis was present in 15/16 probands and 1/9 discovered homozygotes (p < 0.005). Radiologic evidence of arthropathy was seen additionally in 2 asymptomatic discovered homozygotes. The metacarpophalangeal joints and wrists were most commonly involved; severe hip disease occurred in 6. Patients with clinical or radiologic arthropathy were older than patients without. Arthropathy occurred in all 4 female probands, but in none of the 3 female discovered homozygotes. Chondrocalcinosis was seen in 9 subjects but was usually asymptomatic. The arthritis of hemochromatosis may be difficult to differentiate from several other joint diseases, especially calcium pyrophosphate dihydrate deposition disease.
我们回顾了25例血色素沉着症患者(16例先证者和9例发现的纯合子亲属)关节病的临床和影像学特征。15/16例先证者和1/9例发现的纯合子存在临床关节炎(p<0.005)。另外,在2例无症状的发现的纯合子中也发现了关节病的影像学证据。掌指关节和腕关节最常受累;6例出现严重的髋关节疾病。有临床或影像学关节病的患者比无关节病的患者年龄更大。所有4例女性先证者均出现关节病,但3例发现的女性纯合子均未出现。9例患者出现软骨钙质沉着症,但通常无症状。血色素沉着症性关节炎可能难以与其他几种关节疾病相鉴别,尤其是焦磷酸钙二水合物沉积病。