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Hyperpigmentation as a peculiar presentation of mycosis fungoides

Hyperpigmented mycosis fungoides is an extremely rare subtype of mycosis fungoides. It presents as multiple pigmented macules and patches without poikilodermatous changes and characterized by a CD8+ phenotype on immunohistochemistry. This report describes a typical case of hyperpigmented mycosis fun...

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Autores principales: Lu, Ying-Yi, Wu, Chieh-Hsin, Lu, Chun-Ching, Hong, Chien-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726689/
https://www.ncbi.nlm.nih.gov/pubmed/29267458
http://dx.doi.org/10.1590/abd1806-4841.20175544
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author Lu, Ying-Yi
Wu, Chieh-Hsin
Lu, Chun-Ching
Hong, Chien-Hui
author_facet Lu, Ying-Yi
Wu, Chieh-Hsin
Lu, Chun-Ching
Hong, Chien-Hui
author_sort Lu, Ying-Yi
collection PubMed
description Hyperpigmented mycosis fungoides is an extremely rare subtype of mycosis fungoides. It presents as multiple pigmented macules and patches without poikilodermatous changes and characterized by a CD8+ phenotype on immunohistochemistry. This report describes a typical case of hyperpigmented mycosis fungoides in a 62-year-old woman, who presented with a 7-year history of multiple hyperpigmented macules and patches on the trunk and right leg with progression over this half a year. Histology and immunohistochemical staining of skin samples confirmed the diagnosis of mycosis fungoides. She received psoralen plus ultraviolet A (PUVA) therapy. After an 8-week treatment, the erythematous changes cleared without recurrence during a 6-month follow-up period. An intractable hyperpigmented patch should raise the clinical suspicion of mycosis fungoides with sequential skin biopsy.
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spelling pubmed-57266892017-12-18 Hyperpigmentation as a peculiar presentation of mycosis fungoides Lu, Ying-Yi Wu, Chieh-Hsin Lu, Chun-Ching Hong, Chien-Hui An Bras Dermatol Case Report Hyperpigmented mycosis fungoides is an extremely rare subtype of mycosis fungoides. It presents as multiple pigmented macules and patches without poikilodermatous changes and characterized by a CD8+ phenotype on immunohistochemistry. This report describes a typical case of hyperpigmented mycosis fungoides in a 62-year-old woman, who presented with a 7-year history of multiple hyperpigmented macules and patches on the trunk and right leg with progression over this half a year. Histology and immunohistochemical staining of skin samples confirmed the diagnosis of mycosis fungoides. She received psoralen plus ultraviolet A (PUVA) therapy. After an 8-week treatment, the erythematous changes cleared without recurrence during a 6-month follow-up period. An intractable hyperpigmented patch should raise the clinical suspicion of mycosis fungoides with sequential skin biopsy. Sociedade Brasileira de Dermatologia 2017 /pmc/articles/PMC5726689/ /pubmed/29267458 http://dx.doi.org/10.1590/abd1806-4841.20175544 Text en ©2017 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Case Report
Lu, Ying-Yi
Wu, Chieh-Hsin
Lu, Chun-Ching
Hong, Chien-Hui
Hyperpigmentation as a peculiar presentation of mycosis fungoides
title Hyperpigmentation as a peculiar presentation of mycosis fungoides
title_full Hyperpigmentation as a peculiar presentation of mycosis fungoides
title_fullStr Hyperpigmentation as a peculiar presentation of mycosis fungoides
title_full_unstemmed Hyperpigmentation as a peculiar presentation of mycosis fungoides
title_short Hyperpigmentation as a peculiar presentation of mycosis fungoides
title_sort hyperpigmentation as a peculiar presentation of mycosis fungoides
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726689/
https://www.ncbi.nlm.nih.gov/pubmed/29267458
http://dx.doi.org/10.1590/abd1806-4841.20175544
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