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Bilateral Breast Ochronosis: a Case Report

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 o...

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Detalles Bibliográficos
Autores principales: AbdulKarim, Fatema A.J., Ibrahim, Safwat M., Hill, Arnold AD, Ajmal, Nadeem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340040/
https://www.ncbi.nlm.nih.gov/pubmed/34381863
http://dx.doi.org/10.1016/j.jpra.2021.06.005
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author AbdulKarim, Fatema A.J.
Ibrahim, Safwat M.
Hill, Arnold AD
Ajmal, Nadeem
author_facet AbdulKarim, Fatema A.J.
Ibrahim, Safwat M.
Hill, Arnold AD
Ajmal, Nadeem
author_sort AbdulKarim, Fatema A.J.
collection PubMed
description 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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spelling pubmed-83400402021-08-10 Bilateral Breast Ochronosis: a Case Report AbdulKarim, Fatema A.J. Ibrahim, Safwat M. Hill, Arnold AD Ajmal, Nadeem JPRAS Open Case Report 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. Elsevier 2021-06-18 /pmc/articles/PMC8340040/ /pubmed/34381863 http://dx.doi.org/10.1016/j.jpra.2021.06.005 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
AbdulKarim, Fatema A.J.
Ibrahim, Safwat M.
Hill, Arnold AD
Ajmal, Nadeem
Bilateral Breast Ochronosis: a Case Report
title Bilateral Breast Ochronosis: a Case Report
title_full Bilateral Breast Ochronosis: a Case Report
title_fullStr Bilateral Breast Ochronosis: a Case Report
title_full_unstemmed Bilateral Breast Ochronosis: a Case Report
title_short Bilateral Breast Ochronosis: a Case Report
title_sort bilateral breast ochronosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340040/
https://www.ncbi.nlm.nih.gov/pubmed/34381863
http://dx.doi.org/10.1016/j.jpra.2021.06.005
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