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Dyschromatosis Symmetrica Hereditaria of Late Onset?

Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo- and hyperpigmented macules of varying sizes on the dorsal of the extremities with reticulated pattern. This paper presents a...

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Autores principales: Gaiewski, Caroline Balvedi, Zuneda Serafini, Sergio, Werner, Betina, Deonizio, Janyana M. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006555/
https://www.ncbi.nlm.nih.gov/pubmed/24826352
http://dx.doi.org/10.1155/2014/639537
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author Gaiewski, Caroline Balvedi
Zuneda Serafini, Sergio
Werner, Betina
Deonizio, Janyana M. D.
author_facet Gaiewski, Caroline Balvedi
Zuneda Serafini, Sergio
Werner, Betina
Deonizio, Janyana M. D.
author_sort Gaiewski, Caroline Balvedi
collection PubMed
description Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo- and hyperpigmented macules of varying sizes on the dorsal of the extremities with reticulated pattern. This paper presents a female patient with typical dermatological lesions, but only diagnosed in adulthood. It is necessary to perform differential diagnosis with other pigmentary disorders. This entity is not very common in South America, and the vast majority of cases were described in Japanese population. Since it is a benign disease, it is important to be aware of this diagnosis in order to establish the correct conduct for these patients.
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spelling pubmed-40065552014-05-13 Dyschromatosis Symmetrica Hereditaria of Late Onset? Gaiewski, Caroline Balvedi Zuneda Serafini, Sergio Werner, Betina Deonizio, Janyana M. D. Case Rep Dermatol Med Case Report Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo- and hyperpigmented macules of varying sizes on the dorsal of the extremities with reticulated pattern. This paper presents a female patient with typical dermatological lesions, but only diagnosed in adulthood. It is necessary to perform differential diagnosis with other pigmentary disorders. This entity is not very common in South America, and the vast majority of cases were described in Japanese population. Since it is a benign disease, it is important to be aware of this diagnosis in order to establish the correct conduct for these patients. Hindawi Publishing Corporation 2014 2014-02-04 /pmc/articles/PMC4006555/ /pubmed/24826352 http://dx.doi.org/10.1155/2014/639537 Text en Copyright © 2014 Caroline Balvedi Gaiewski et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gaiewski, Caroline Balvedi
Zuneda Serafini, Sergio
Werner, Betina
Deonizio, Janyana M. D.
Dyschromatosis Symmetrica Hereditaria of Late Onset?
title Dyschromatosis Symmetrica Hereditaria of Late Onset?
title_full Dyschromatosis Symmetrica Hereditaria of Late Onset?
title_fullStr Dyschromatosis Symmetrica Hereditaria of Late Onset?
title_full_unstemmed Dyschromatosis Symmetrica Hereditaria of Late Onset?
title_short Dyschromatosis Symmetrica Hereditaria of Late Onset?
title_sort dyschromatosis symmetrica hereditaria of late onset?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006555/
https://www.ncbi.nlm.nih.gov/pubmed/24826352
http://dx.doi.org/10.1155/2014/639537
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