Araki Kentaro, Sudo Akihiro, Hasegawa Masahiro, Uchida Atsumasa
Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
J Clin Rheumatol. 2009 Apr;15(3):138-40. doi: 10.1097/RHU.0b013e31819e6b41.
Ochronotic arthropathy is a manifestation of long-standing alkaptonuria, a rare hereditary metabolic disorder characterized by the absence of the enzyme homogentisic acid oxidase. We describe a patient who developed rapidly progressive destructive ochronotic arthropathy in his knee and hip joints and underwent successful bilateral total knee and hip arthroplasties.
褐黄病性关节病是长期存在的尿黑酸尿症的一种表现,尿黑酸尿症是一种罕见的遗传性代谢紊乱疾病,其特征是缺乏尿黑酸氧化酶。我们描述了一名患者,其膝关节和髋关节出现了快速进展的破坏性褐黄病性关节病,并成功接受了双侧全膝关节和全髋关节置换术。