Abstract |
Ochronosis is a syndrome characterized by bluish black discoloration due to the deposition of polymerized products of homogentisic acid (HGA) in the connective tissues. The endogenous variety ( alkaptonuria), is a rare autosomal recessive metabolic disorder. The disorder is manifested by deficiency of the enzyme homogentisate 1,2-dioxygenase. The characteristic of the condition is a triad of pigmentation of skin, cartilage, and sclera; ochronotic arthropathies and homogentisic aciduria (resulting in darkening of urine). More rarely, it may affect the breast. This rare and interesting case of a woman with ochronosis of both breasts and chest wall, prompted us to write this case report.
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Authors | Fatema A J AbdulKarim, Safwat M Ibrahim, Arnold Ad Hill, Nadeem Ajmal |
Journal | JPRAS open
(JPRAS Open)
Vol. 30
Pg. 23-28
(Dec 2021)
ISSN: 2352-5878 [Electronic] Netherlands |
PMID | 34381863
(Publication Type: Case Reports)
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Copyright | © 2021 The Authors. |