| Literature DB >> 35415103 |
Syam G1, John Thayyil John1, Dileep Sasidharan Nair1, Shikhar Yadav1, Joice Varghese1, Jamsheed T1.
Abstract
Introduction: Alkaptonuria is a rare autosomal recessive metabolic disorder characterized by accumulation of homogentisic acid (HGA) due to an inherited deficiency of the enzyme HGA oxidase. Unlike rheumatoid arthritis which affects the small joints of the hands and feet, ochronotic arthropathy predominantly involves the large weight-bearing joints such as hips, knees, and spine. The knee is the most common joint to be affected. Ochronotic arthropathy is usually managed conservatively, but for severely affected hip and knee joints, replacement is considered. Case Report: This report describes a case of 57-year-old male who presented with bilateral knee osteoarthritis who was incidentally diagnosed with ochronosis intraoperatively during total knee arthroplasty, its challenges faced and post-operative functional outcome after 18 months follow-up.Entities:
Keywords: Alkaptonuria; autosomal recessive; ochronosis; ochronotic arthropathy; total knee arthroplasty
Year: 2021 PMID: 35415103 PMCID: PMC8930298 DOI: 10.13107/jocr.2021.v11.i10.2464
Source DB: PubMed Journal: J Orthop Case Rep ISSN: 2250-0685
Figure 1Pre-operative radiographs of both the knees suggesting features of osteoarthritis
Figure 2Ochronotic involvement of sub cutaneous tissue and synovim with synovial hypertrophy
Figure 3Black articular cartilage of femur and patella. Sub chondral bone in areas of cartilage defect is normalin appearance
Figure 4Bone cuts and excised synovium
Figur 5Post-operative anteroposterior radiographs of both knees
Figure 6Post-operative lateral radiographs of both knees
Figure 7Biopsy specimen showing normal tissue above and pigmented macrophage and inflammatory cells below
Figure 8Pigment deposition in the sclera – Osler’s sign
Figure 9Pigmentation over thenear and hypo thenar eminence