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Syndrome in question: Gorlin-Goltz syndrome
The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormalities. Due to the wide clinical spectrum, treatment...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999122/ https://www.ncbi.nlm.nih.gov/pubmed/27579759 http://dx.doi.org/10.1590/abd1806-4841.20164428 |
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author | Ribeiro, Pauline Lyrio de Souza Filho, João Basílio de Abreu, Karina Demoner Brezinscki, Marisa Simon Pignaton, Christine Chambo |
author_facet | Ribeiro, Pauline Lyrio de Souza Filho, João Basílio de Abreu, Karina Demoner Brezinscki, Marisa Simon Pignaton, Christine Chambo |
author_sort | Ribeiro, Pauline Lyrio |
collection | PubMed |
description | The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormalities. Due to the wide clinical spectrum, treatment and management of its modalities are not standardized and should be individualized and monitored by a multidisciplinary team. We report a typical case in a 30-year-old man with multiple basal cell carcinomas, keratotic pits of palmar creases and bifid ribs, with a history of several corrective surgeries for keratocystic odontogenic tumors, among other lesions characteristic of the syndrome. |
format | Online Article Text |
id | pubmed-4999122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-49991222016-08-29 Syndrome in question: Gorlin-Goltz syndrome Ribeiro, Pauline Lyrio de Souza Filho, João Basílio de Abreu, Karina Demoner Brezinscki, Marisa Simon Pignaton, Christine Chambo An Bras Dermatol Syndrome in Question The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an uncommon disorder caused by a mutation in Patched, tumor suppressor gene. It is mainly characterized by numerous early onset basal cell carcinomas, odontogenic cysts of jaw and skeletal abnormalities. Due to the wide clinical spectrum, treatment and management of its modalities are not standardized and should be individualized and monitored by a multidisciplinary team. We report a typical case in a 30-year-old man with multiple basal cell carcinomas, keratotic pits of palmar creases and bifid ribs, with a history of several corrective surgeries for keratocystic odontogenic tumors, among other lesions characteristic of the syndrome. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC4999122/ /pubmed/27579759 http://dx.doi.org/10.1590/abd1806-4841.20164428 Text en ©2016 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited. |
spellingShingle | Syndrome in Question Ribeiro, Pauline Lyrio de Souza Filho, João Basílio de Abreu, Karina Demoner Brezinscki, Marisa Simon Pignaton, Christine Chambo Syndrome in question: Gorlin-Goltz syndrome |
title | Syndrome in question: Gorlin-Goltz syndrome
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title_full | Syndrome in question: Gorlin-Goltz syndrome
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title_fullStr | Syndrome in question: Gorlin-Goltz syndrome
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title_full_unstemmed | Syndrome in question: Gorlin-Goltz syndrome
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title_short | Syndrome in question: Gorlin-Goltz syndrome
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title_sort | syndrome in question: gorlin-goltz syndrome |
topic | Syndrome in Question |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999122/ https://www.ncbi.nlm.nih.gov/pubmed/27579759 http://dx.doi.org/10.1590/abd1806-4841.20164428 |
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