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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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. |
format | Online Article Text |
id | pubmed-8340040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT abdulkarimfatemaaj bilateralbreastochronosisacasereport AT ibrahimsafwatm bilateralbreastochronosisacasereport AT hillarnoldad bilateralbreastochronosisacasereport AT ajmalnadeem bilateralbreastochronosisacasereport |