Bilateral Breast Ochronosis: a Case Report
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 de...
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Elsevier
2021
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oai:doaj.org-article:06cabf0603c142f4a4a1622d3102325d2021-12-02T05:02:00ZBilateral Breast Ochronosis: a Case Report2352-587810.1016/j.jpra.2021.06.005https://doaj.org/article/06cabf0603c142f4a4a1622d3102325d2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2352587821000590https://doaj.org/toc/2352-5878ABSTRACT: 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.Fatema A.J. AbdulKarimSafwat M. IbrahimArnold AD HillNadeem AjmalElsevierarticleOchronosisAlkaptonuriaHomogentisic acidBreast ochronosisMastectomySurgeryRD1-811ENJPRAS Open, Vol 30, Iss , Pp 23-28 (2021) |
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Ochronosis Alkaptonuria Homogentisic acid Breast ochronosis Mastectomy Surgery RD1-811 |
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Ochronosis Alkaptonuria Homogentisic acid Breast ochronosis Mastectomy Surgery RD1-811 Fatema A.J. AbdulKarim Safwat M. Ibrahim Arnold AD Hill Nadeem Ajmal Bilateral Breast Ochronosis: a Case Report |
description |
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. |
format |
article |
author |
Fatema A.J. AbdulKarim Safwat M. Ibrahim Arnold AD Hill Nadeem Ajmal |
author_facet |
Fatema A.J. AbdulKarim Safwat M. Ibrahim Arnold AD Hill Nadeem Ajmal |
author_sort |
Fatema A.J. AbdulKarim |
title |
Bilateral Breast Ochronosis: a Case Report |
title_short |
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_sort |
bilateral breast ochronosis: a case report |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/06cabf0603c142f4a4a1622d3102325d |
work_keys_str_mv |
AT fatemaajabdulkarim bilateralbreastochronosisacasereport AT safwatmibrahim bilateralbreastochronosisacasereport AT arnoldadhill bilateralbreastochronosisacasereport AT nadeemajmal bilateralbreastochronosisacasereport |
_version_ |
1718400751541157888 |