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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Format: | Article |
Language: | English |
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Sociedade Brasileira de Dermatologia
2015-10-01
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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. |
first_indexed | 2024-12-20T09:41:57Z |
format | Article |
id | doaj.art-e7b967e61f9e4261b893e1cae8b6a5a1 |
institution | Directory Open Access Journal |
issn | 0365-0596 |
language | English |
last_indexed | 2024-12-20T09:41:57Z |
publishDate | 2015-10-01 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | Article |
series | Anais Brasileiros de Dermatologia |
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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