Syndrome in question

AbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded a...

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Main Authors: Catharina Maria Freire de Lucena Pousa, Fernanda Guedes Lavorato, Fernanda Valente Rehfeldt, Danielle Mann, Maria de Fátima Gonçalves Scotelaro Alves
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2015-10-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000500759&tlng=en
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author Catharina Maria Freire de Lucena Pousa
Fernanda Guedes Lavorato
Fernanda Valente Rehfeldt
Danielle Mann
Maria de Fátima Gonçalves Scotelaro Alves
author_facet Catharina Maria Freire de Lucena Pousa
Fernanda Guedes Lavorato
Fernanda Valente Rehfeldt
Danielle Mann
Maria de Fátima Gonçalves Scotelaro Alves
author_sort Catharina Maria Freire de Lucena Pousa
collection DOAJ
description AbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. We report the case of a patient who, after a ten-year diagnosis of colorectal cancer, presented with multiple sebaceous neoplasms.
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spelling doaj.art-e7b967e61f9e4261b893e1cae8b6a5a12022-12-21T19:44:52ZengSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia0365-05962015-10-0190575976110.1590/abd1806-4841.20153193Syndrome in questionCatharina Maria Freire de Lucena PousaFernanda Guedes LavoratoFernanda Valente RehfeldtDanielle MannMaria de Fátima Gonçalves Scotelaro AlvesAbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. We report the case of a patient who, after a ten-year diagnosis of colorectal cancer, presented with multiple sebaceous neoplasms.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000500759&tlng=enSebaceous gland neoplasmsColorectal neoplasms, hereditary nonpolyposisSkin NeoplasmsSyndromeMuir-Torre Syndrome
spellingShingle Catharina Maria Freire de Lucena Pousa
Fernanda Guedes Lavorato
Fernanda Valente Rehfeldt
Danielle Mann
Maria de Fátima Gonçalves Scotelaro Alves
Syndrome in question
Anais Brasileiros de Dermatologia
Sebaceous gland neoplasms
Colorectal neoplasms, hereditary nonpolyposis
Skin Neoplasms
Syndrome
Muir-Torre Syndrome
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 Sebaceous gland neoplasms
Colorectal neoplasms, hereditary nonpolyposis
Skin Neoplasms
Syndrome
Muir-Torre Syndrome
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000500759&tlng=en
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