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Syndrome in question

Morbihan Syndrome is a rare entity with unknown etiology. It is clinically characterized by chronic erythematous edema on the face - especially in the middle and upper third of the face - and creates abnormal facial contours that are initially intermitent but become permanent with the development of...

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Autores principales: Rebellato, Priscila Regina Orso, Rezende, Camila Makino, Battaglin, Eveline Roesler, de Lima, Brunno Zeni, Fillus Neto, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689086/
https://www.ncbi.nlm.nih.gov/pubmed/26734879
http://dx.doi.org/10.1590/abd1806-4841.20153818
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author Rebellato, Priscila Regina Orso
Rezende, Camila Makino
Battaglin, Eveline Roesler
de Lima, Brunno Zeni
Fillus Neto, Jose
author_facet Rebellato, Priscila Regina Orso
Rezende, Camila Makino
Battaglin, Eveline Roesler
de Lima, Brunno Zeni
Fillus Neto, Jose
author_sort Rebellato, Priscila Regina Orso
collection PubMed
description Morbihan Syndrome is a rare entity with unknown etiology. It is clinically characterized by chronic erythematous edema on the face - especially in the middle and upper third of the face - and creates abnormal facial contours that are initially intermitent but become permanent with the development of the syndrome. The histopathology is nonspecific and its therapy is a major challenge due to poor response to the various treatment options. We present the case of a male patient with a five-month-history of disease.
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spelling pubmed-46890862015-12-28 Syndrome in question Rebellato, Priscila Regina Orso Rezende, Camila Makino Battaglin, Eveline Roesler de Lima, Brunno Zeni Fillus Neto, Jose An Bras Dermatol Syndrome in Question Morbihan Syndrome is a rare entity with unknown etiology. It is clinically characterized by chronic erythematous edema on the face - especially in the middle and upper third of the face - and creates abnormal facial contours that are initially intermitent but become permanent with the development of the syndrome. The histopathology is nonspecific and its therapy is a major challenge due to poor response to the various treatment options. We present the case of a male patient with a five-month-history of disease. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4689086/ /pubmed/26734879 http://dx.doi.org/10.1590/abd1806-4841.20153818 Text en ©2015 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Syndrome in Question
Rebellato, Priscila Regina Orso
Rezende, Camila Makino
Battaglin, Eveline Roesler
de Lima, Brunno Zeni
Fillus Neto, Jose
Syndrome in question
title Syndrome in question
title_full Syndrome in question
title_fullStr Syndrome in question
title_full_unstemmed Syndrome in question
title_short Syndrome in question
title_sort syndrome in question
topic Syndrome in Question
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689086/
https://www.ncbi.nlm.nih.gov/pubmed/26734879
http://dx.doi.org/10.1590/abd1806-4841.20153818
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