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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...

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Detalles Bibliográficos
Autores principales: Ribeiro, Pauline Lyrio, de Souza Filho, João Basílio, de Abreu, Karina Demoner, Brezinscki, Marisa Simon, Pignaton, Christine Chambo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
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.
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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
title_full Syndrome in question: Gorlin-Goltz syndrome
title_fullStr Syndrome in question: Gorlin-Goltz syndrome
title_full_unstemmed Syndrome in question: Gorlin-Goltz syndrome
title_short Syndrome in question: Gorlin-Goltz syndrome
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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