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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...
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/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. |
format | Online Article Text |
id | pubmed-4689086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT rebellatopriscilareginaorso syndromeinquestion AT rezendecamilamakino syndromeinquestion AT battaglinevelineroesler syndromeinquestion AT delimabrunnozeni syndromeinquestion AT fillusnetojose syndromeinquestion |