Ochronotic arthropathy: diagnosis and management: a critical review.

Abstract

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.

• Authors: Emmanouil Drakoulakis, Dimitrios Varvitsiotis, Georgioss Psarea, John Feroussis
• Journal: American journal of orthopedics (Belle Mead, N.J.) (Am J Orthop (Belle Mead NJ)) Vol. 41 Issue 2 Pg. 80-3 (Feb 2012) ISSN: 1934-3418 [Electronic] United States
• PMID: 22482092 (Publication Type: Case Reports, Journal Article, Review)

Topics

• Alkaptonuria (complications, diagnosis, surgery)
• Arthroplasty, Replacement (methods)
• Exercise Therapy
• Humans
• Joint Diseases (etiology, pathology, therapy)
• Male
• Middle Aged
• Ochronosis (complications, diagnosis, surgery)
• Postoperative Complications
• Prosthesis Failure
• Range of Motion, Articular
• Recovery of Function
• Shoulder Joint (pathology, physiopathology, surgery)
• Treatment Outcome