Pierce Todd P, Issa Kimona, Ramirez Andres, Sclafani Salvatore, Harwin Steven F, Scillia Anthony J, Rifai Aiman, McInerney Vincent K
Department of Orthopaedics, Seton Hall University, School of Health, and Medical Sciences, South Orange, NJ.
New York Medical College, Department of Orthopaedic Surgery, Valhalla, New York.
Surg Technol Int. 2016 Oct 26;29:261-264.
Alkaptonuria is a rare hereditary metabolic disorder that leads to the accumulation of homogentisic acid accumulation and weakens the collagen, creating fissuring and articular cartilage degeneration. Therefore, we are reporting a multicenter case series of three patients (four arthroplasties) who presented with signs and symptoms of ochronotic arthropathy-and eventually underwent total knee arthroplasty (TKA)-and provide a review of the current literature on total joint arthroplasty in ochronotic osteoarthritis. Each patient achieved excellent Knee Society Scores (KSS) after at least a five-year follow-up-regardless of receiving cemented or cementless prostheses-and suffered no complications. There have been a number of case reports published on patients who had TKA and were found to have a diagnosis of ochronosis. We believe that surgery for symptomatic patients who are surgical candidates for TKA should not be delayed for concerns of complications. However, future studies should compare outcomes to those who undergo TKA without ochronotic arthropathy.
黑尿症是一种罕见的遗传性代谢紊乱疾病,会导致尿黑酸积累,并使胶原蛋白变弱,从而产生裂隙和关节软骨退变。因此,我们报告了一个多中心病例系列,其中三名患者(接受了四次关节置换术)出现了褐黄病性关节病的体征和症状,并最终接受了全膝关节置换术(TKA),并对当前关于褐黄病性骨关节炎全关节置换术的文献进行了综述。每位患者在至少五年的随访后均获得了优异的膝关节协会评分(KSS),无论使用的是骨水泥型还是非骨水泥型假体,且均未出现并发症。已有多篇关于接受TKA且被诊断为褐黄病的患者的病例报告发表。我们认为,对于有症状且适合TKA手术的患者,不应因担心并发症而延迟手术。然而,未来的研究应将结果与未患褐黄病性关节病而接受TKA的患者进行比较。