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Granulomatous mycosis fungoides - A diagnostic challenge
Granulomatous mycosis fungoides is a rare subtype of T-cell cutaneous lymphoma. Due to its clinical heterogenicity the diagnosis is delayed and based on histopathological and immuno-histochemical findings, sometimes requiring gene rearrangement studies for confirmation. We report the case of a patie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560545/ https://www.ncbi.nlm.nih.gov/pubmed/26375225 http://dx.doi.org/10.1590/abd1806-4841.20153460 |
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author | Pousa, Catharina Maria Freire de Lucena Nery, Natália Solon Mann, Danielle Obadia, Daniel Lago Alves, Maria de Fátima Gonçalves Scotelaro |
author_facet | Pousa, Catharina Maria Freire de Lucena Nery, Natália Solon Mann, Danielle Obadia, Daniel Lago Alves, Maria de Fátima Gonçalves Scotelaro |
author_sort | Pousa, Catharina Maria Freire de Lucena |
collection | PubMed |
description | Granulomatous mycosis fungoides is a rare subtype of T-cell cutaneous lymphoma. Due to its clinical heterogenicity the diagnosis is delayed and based on histopathological and immuno-histochemical findings, sometimes requiring gene rearrangement studies for confirmation. We report the case of a patient who was submitted to several biopsies before diagnostic conclusion. |
format | Online Article Text |
id | pubmed-4560545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-45605452015-09-09 Granulomatous mycosis fungoides - A diagnostic challenge Pousa, Catharina Maria Freire de Lucena Nery, Natália Solon Mann, Danielle Obadia, Daniel Lago Alves, Maria de Fátima Gonçalves Scotelaro An Bras Dermatol Dermatopathology Granulomatous mycosis fungoides is a rare subtype of T-cell cutaneous lymphoma. Due to its clinical heterogenicity the diagnosis is delayed and based on histopathological and immuno-histochemical findings, sometimes requiring gene rearrangement studies for confirmation. We report the case of a patient who was submitted to several biopsies before diagnostic conclusion. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4560545/ /pubmed/26375225 http://dx.doi.org/10.1590/abd1806-4841.20153460 Text en © 2015 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 | Dermatopathology Pousa, Catharina Maria Freire de Lucena Nery, Natália Solon Mann, Danielle Obadia, Daniel Lago Alves, Maria de Fátima Gonçalves Scotelaro Granulomatous mycosis fungoides - A diagnostic challenge |
title | Granulomatous mycosis fungoides - A diagnostic challenge |
title_full | Granulomatous mycosis fungoides - A diagnostic challenge |
title_fullStr | Granulomatous mycosis fungoides - A diagnostic challenge |
title_full_unstemmed | Granulomatous mycosis fungoides - A diagnostic challenge |
title_short | Granulomatous mycosis fungoides - A diagnostic challenge |
title_sort | granulomatous mycosis fungoides - a diagnostic challenge |
topic | Dermatopathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560545/ https://www.ncbi.nlm.nih.gov/pubmed/26375225 http://dx.doi.org/10.1590/abd1806-4841.20153460 |
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