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一例黑尿症——超声检查结果

A case of alkaptonuria - ultrasonographic findings.

作者信息

Damian Laura Otilia, Felea Ioana, Boloşiu Călin, Botar-Jid Carolina, Fodor Daniela, Rednic Simona

机构信息

Rheumatology Department, Emergency Clinical County Hospital, Cluj-Napoca, Romania; Email:

出版信息

Med Ultrason. 2013 Dec;15(4):321-5. doi: 10.11152/mu.2013.2066.154.lod2.

Abstract

Alkaptonuria is a rare disease with autosomal recessive inheritance and variable expression. The weight-bearing joint involvement and spondylitis-like vertebral changes occur only after the 3rd decade. Musculoskeletal ultrasonographic findings in alkaptonuria were only rarely described, consisting mainly into enthesopathy and non-synovial tendon degeneration. We present the case of a 50 years old man with alkaptonuria and discuss the ultrasonographic findings and the relationship of the disease with chondrocalcinosis. The tendinous and synovial aspect may be peculiar and it could therefore allow recognition and screening for alkaptonuria, along with clinical and radiologic data.

摘要

黑尿症是一种罕见的常染色体隐性遗传病,表现多样。负重关节受累和脊柱炎样椎体改变仅在30岁以后出现。黑尿症的肌肉骨骼超声检查结果很少被描述,主要表现为附着点病和非滑膜肌腱退变。我们报告一例50岁男性黑尿症患者,并讨论其超声检查结果以及该疾病与软骨钙质沉着症的关系。肌腱和滑膜方面可能具有特殊性,因此结合临床和放射学数据,它可用于黑尿症的识别和筛查。

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