| Literature DB >> 27817975 |
Sinan Karaoğlu1, Fatih Karaaslan2, Musa Uğur Mermerkaya2.
Abstract
Alkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogentisic acid oxidase, which results in excess homogentisic acid (HGA) levels. Homogentisic acid and its oxidation products can accumulate in hyaline cartilage, tendons, and ligaments. A 55-year-old male was admitted complaining of worsening chronic pain in his left knee. A radiographic evaluation showed tricompartmental end- stage osteoarthritis. A cemented total knee replacement was performed. At the 10-year follow-up, he had returned to full activity, had no knee pain, and was very satisfied with the outcome. No abnormality was observed in the femoral, tibial, or patellar components on radiography. We believe that total knee replacement is a good option in a patient with marked degenerative arthritis secondary to ochronotic arthritis.Entities:
Keywords: Alkaptonuria; Arthroplasty; Knee joint; Ochronotic arthropathy
Mesh:
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Year: 2016 PMID: 27817975 PMCID: PMC6197303 DOI: 10.1016/j.aott.2016.08.018
Source DB: PubMed Journal: Acta Orthop Traumatol Turc ISSN: 1017-995X Impact factor: 1.511
Fig. 1Preoperative radiographs showing osteoarthritic changes.
Fig. 2Pigmentation of sclerae and skin of peri-orbital area.
Fig. 3Macroscopic findings at surgery, showing black pigmentation in the synovium and articular surfaces.
Fig. 4Radiographs following total knee arthroplasty.
Fig. 5Anteroposterior and lateral radiograph of same knee at 10th year postoperatively, with stable components.