Cetinus Ercan, Cever Ilhan, Kural Cemal, Erturk Haldun, Akyildiz Mustafa
Faculty of Medicine, Department of Orthopedics, University of Kahramanmaras Sutcu Imam, Kahramanmaras, 46050, Turkey.
Rheumatol Int. 2005 Aug;25(6):465-8. doi: 10.1007/s00296-004-0538-x. Epub 2004 Dec 3.
Alkoptunuria is an inherited autosomal recessive metabolic disorder which is caused by the lack of homogentisic acid-oxidase enzyme. It is associated with various systemic abnormalities and related to the deposition of homogentisic acid pigment in connective tissues. These pigmentary changes are termed "ochronosis". We describe two patients with ochronotic arthritis who presented with advanced degenerative changes in the lumbo-sacral spine, knee and hip. The literature, differential diagnosis and management of this rare condition are reviewed in this article.
褐黄病是一种常染色体隐性遗传代谢紊乱疾病,由尿黑酸氧化酶缺乏引起。它与多种全身异常有关,并与尿黑酸色素在结缔组织中的沉积有关。这些色素变化被称为“褐黄病”。我们描述了两名患有褐黄病性关节炎的患者,他们的腰骶椎、膝关节和髋关节出现了晚期退行性改变。本文对这种罕见疾病的文献、鉴别诊断和治疗进行了综述。