Jasper Jorrit, Metsaars Wieneke, Jansen Joris
Department of Orthopedics, Alrijne Ziekenhuis, Leiderdorp, The Netherlands.
BMJ Case Rep. 2016 May 20;2016:bcr2016215412. doi: 10.1136/bcr-2016-215412.
Ochronosis is a rare autosomal recessive metabolic disease caused by homogentisic acid oxidase enzyme deficiency. High homogentisic acid levels will eventually result in black deposits in skin, sclerae, connective tissues and urine (alkaptonuria). It can lead to early degeneration of connective tissues and cartilage. Ochronosis can damage normal cartilage, leading to secondary osteoarthritis. The diagnosis is often delayed because of its low prevalence and non-specific early symptoms. In our patient, the secondary osteoarthritis due to ochronosis deposits in the cartilage was treated by total knee arthroplasty, with good clinical outcome. This article reports the first case of ochronosis with secondary osteoarthritis of the knee in a patient previously diagnosed with cryptogenic organising pneumonia (COP).
褐黄病是一种罕见的常染色体隐性代谢疾病,由尿黑酸氧化酶缺乏引起。高尿黑酸水平最终会导致皮肤、巩膜、结缔组织和尿液中出现黑色沉积物(尿黑酸尿症)。它可导致结缔组织和软骨早期退变。褐黄病会损害正常软骨,导致继发性骨关节炎。由于其发病率低且早期症状不具特异性,诊断往往会延迟。在我们的患者中,因褐黄病沉积物在软骨中导致的继发性骨关节炎通过全膝关节置换术进行治疗,临床效果良好。本文报告了首例先前被诊断为隐源性机化性肺炎(COP)的患者出现褐黄病伴膝关节继发性骨关节炎的病例。