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尿黑酸尿症性褐黄病:基于病例的综述。

Alkaptonuric Ochronosis: A case-based review.

出版信息

Acta Orthop Belg. 2024 Jun;90(2):343-348. doi: 10.52628/90.2.12403.

Abstract

Alkaptonuria (AKU) is an extremely rare autosomal recessive metabolic disorder caused by deficiency of homogentisic acid oxidase and resulting in accumulation of homogentisic acid in collagenous structures. It is characterized by a triad of homogentisic aciduria, bluish-black discoloration of connective tissues (ochronosis) and arthropathy of large weight bearing joints. We report on a middle-aged female patient with bilateral severe ochronotic arthritis of both hips and shoulder joints requiring total joint replacements as staged procedures which were done without complications offering a complete pain relief and a satisfactory clinical and functional outcome. Ochronosis can cause severe arthropathy of peripheral joints. Multiple joint affection is common. Total joint replacement can yield persistent pain relief with complete functional recovery in patients with severe ochronotic arthropathy.

摘要

尿黑酸尿症(AKU)是一种极为罕见的常染色体隐性遗传代谢紊乱疾病,由 HOMOGENTISIC ACID OXIDASE 缺乏引起,导致 HOMOGENTISIC ACID 在胶原结构中积累。其特征为 HOMOGENTISIC ACIDURIA、结缔组织的蓝黑色变色(褐黄病)和大承重关节的关节炎三联征。我们报告了一位中年女性患者,双侧髋关节和肩关节双侧严重褐黄病性关节炎,需要分期进行全关节置换术,手术过程无并发症,提供了完全的疼痛缓解以及满意的临床和功能结果。褐黄病可导致外周关节严重关节炎。多关节受累很常见。对于严重褐黄病性关节炎患者,全关节置换术可持久缓解疼痛,完全恢复功能。

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