Case Reports
Ochronotic Arthropathy: Diagnosis and Management—A Critical Review
Am J Orthop. 2012 February;41(2):80-83
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Emmanouil Drakoulakis, MD, Dimitrios Varvitsiotis, MD, Georgios Psareas, MD, and John Feroussis, MD, PhD
Alkaptonuria, a rare hereditary metabolic disorder, is characterized by accumulation of homogentisic acid in the connective tissues resulting from lack of the enzyme homogentisic acid oxidase. Ochronosis, dark pigmentation of connective tissues, is the musculoskeletal manifestation of alkaptonuria.
In this article, we report the case of a 53-year-old man who had ochronotic arthropathy and advanced degenerative changes in the shoulders managed with bilateral total shoulder arthroplasty. Three-year follow-up results were satisfactory: good range of motion, no pain, and no signs of prosthesis loosening. Shoulder function was significantly improved after surgery, as documented by Constant scores.
This case suggests that shoulder prosthesis results are not affected by alkaptonuria.