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Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer

The Muir‐Torre Syndrome is a rare genodermatosis, defined by the occurrence of sebaceous neoplasia and internal malignancies and caused by mutations in the mismatch repair gene. We describe the case of 58‐year‐old man who, over the course of several years, had multiple skin lesions and colon cancer....

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Autores principales: Ben Rejeb, Mohamed, Mokni, Sana, Ben Rejeb, Maha, Abdelmoula, Nihed, Sriha, Baderedine, Khochteli, Habib, Denguezli, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898818/
https://www.ncbi.nlm.nih.gov/pubmed/35280107
http://dx.doi.org/10.1002/ccr3.5537
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author Ben Rejeb, Mohamed
Mokni, Sana
Ben Rejeb, Maha
Abdelmoula, Nihed
Sriha, Baderedine
Khochteli, Habib
Denguezli, Mohamed
author_facet Ben Rejeb, Mohamed
Mokni, Sana
Ben Rejeb, Maha
Abdelmoula, Nihed
Sriha, Baderedine
Khochteli, Habib
Denguezli, Mohamed
author_sort Ben Rejeb, Mohamed
collection PubMed
description The Muir‐Torre Syndrome is a rare genodermatosis, defined by the occurrence of sebaceous neoplasia and internal malignancies and caused by mutations in the mismatch repair gene. We describe the case of 58‐year‐old man who, over the course of several years, had multiple skin lesions and colon cancer. The syndrome was diagnosed using Sanger sequencing, which allowed us to find the causative mutation.
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spelling pubmed-88988182022-03-11 Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer Ben Rejeb, Mohamed Mokni, Sana Ben Rejeb, Maha Abdelmoula, Nihed Sriha, Baderedine Khochteli, Habib Denguezli, Mohamed Clin Case Rep Clinical Images The Muir‐Torre Syndrome is a rare genodermatosis, defined by the occurrence of sebaceous neoplasia and internal malignancies and caused by mutations in the mismatch repair gene. We describe the case of 58‐year‐old man who, over the course of several years, had multiple skin lesions and colon cancer. The syndrome was diagnosed using Sanger sequencing, which allowed us to find the causative mutation. John Wiley and Sons Inc. 2022-03-06 /pmc/articles/PMC8898818/ /pubmed/35280107 http://dx.doi.org/10.1002/ccr3.5537 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Images
Ben Rejeb, Mohamed
Mokni, Sana
Ben Rejeb, Maha
Abdelmoula, Nihed
Sriha, Baderedine
Khochteli, Habib
Denguezli, Mohamed
Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title_full Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title_fullStr Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title_full_unstemmed Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title_short Multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
title_sort multiple sebaceous tumors in a 58‐year‐old man with colorectal cancer
topic Clinical Images
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898818/
https://www.ncbi.nlm.nih.gov/pubmed/35280107
http://dx.doi.org/10.1002/ccr3.5537
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