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BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy

BACKGROUND: BRCA1 associated-protein 1 (BAP1) tumor predisposition syndrome is associated with an increased risk for malignant mesotheliomas, uveal and cutaneous melanomas, renal cell carcinomas, and singular cutaneous lesions. The latter are referred to as BAP1-inactivated melanocytic tumors (BIMTs...

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Autores principales: Soares de Sá, Bianca Costa, de Macedo, Mariana Petaccia, Torrezan, Giovana Tardin, Braga, Juliana Casagrande Tavoloni, Fidalgo, Felipe, Moredo, Luciana Facure, Lellis, Rute, Duprat, João Pereira, Carraro, Dirce Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842488/
https://www.ncbi.nlm.nih.gov/pubmed/31706282
http://dx.doi.org/10.1186/s12885-019-6226-8
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author Soares de Sá, Bianca Costa
de Macedo, Mariana Petaccia
Torrezan, Giovana Tardin
Braga, Juliana Casagrande Tavoloni
Fidalgo, Felipe
Moredo, Luciana Facure
Lellis, Rute
Duprat, João Pereira
Carraro, Dirce Maria
author_facet Soares de Sá, Bianca Costa
de Macedo, Mariana Petaccia
Torrezan, Giovana Tardin
Braga, Juliana Casagrande Tavoloni
Fidalgo, Felipe
Moredo, Luciana Facure
Lellis, Rute
Duprat, João Pereira
Carraro, Dirce Maria
author_sort Soares de Sá, Bianca Costa
collection PubMed
description BACKGROUND: BRCA1 associated-protein 1 (BAP1) tumor predisposition syndrome is associated with an increased risk for malignant mesotheliomas, uveal and cutaneous melanomas, renal cell carcinomas, and singular cutaneous lesions. The latter are referred to as BAP1-inactivated melanocytic tumors (BIMTs). When multiple BIMTs manifest, they are considered potential markers of germline BAP1 mutations. CASE PRESENTATION: Here, we report a novel pathogenic BAP1 germline variant in a family with a history of BIMTs, cutaneous melanomas, and mesotheliomas. We also describe singular pathological aspects of the patient’s BIMT lesions and their correlation with dermoscopic and reflectance confocal microscopy findings. CONCLUSIONS: This knowledge is crucial for the recognition of BIMTs by dermatologists and pathologists, allowing the determination of appropriate management for high-risk patients, such as genetic investigations and screening for potentially aggressive tumors.
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spelling pubmed-68424882019-11-14 BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy Soares de Sá, Bianca Costa de Macedo, Mariana Petaccia Torrezan, Giovana Tardin Braga, Juliana Casagrande Tavoloni Fidalgo, Felipe Moredo, Luciana Facure Lellis, Rute Duprat, João Pereira Carraro, Dirce Maria BMC Cancer Case Report BACKGROUND: BRCA1 associated-protein 1 (BAP1) tumor predisposition syndrome is associated with an increased risk for malignant mesotheliomas, uveal and cutaneous melanomas, renal cell carcinomas, and singular cutaneous lesions. The latter are referred to as BAP1-inactivated melanocytic tumors (BIMTs). When multiple BIMTs manifest, they are considered potential markers of germline BAP1 mutations. CASE PRESENTATION: Here, we report a novel pathogenic BAP1 germline variant in a family with a history of BIMTs, cutaneous melanomas, and mesotheliomas. We also describe singular pathological aspects of the patient’s BIMT lesions and their correlation with dermoscopic and reflectance confocal microscopy findings. CONCLUSIONS: This knowledge is crucial for the recognition of BIMTs by dermatologists and pathologists, allowing the determination of appropriate management for high-risk patients, such as genetic investigations and screening for potentially aggressive tumors. BioMed Central 2019-11-09 /pmc/articles/PMC6842488/ /pubmed/31706282 http://dx.doi.org/10.1186/s12885-019-6226-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Soares de Sá, Bianca Costa
de Macedo, Mariana Petaccia
Torrezan, Giovana Tardin
Braga, Juliana Casagrande Tavoloni
Fidalgo, Felipe
Moredo, Luciana Facure
Lellis, Rute
Duprat, João Pereira
Carraro, Dirce Maria
BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title_full BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title_fullStr BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title_full_unstemmed BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title_short BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
title_sort bap1 tumor predisposition syndrome case report: pathological and clinical aspects of bap1-inactivated melanocytic tumors (bimts), including dermoscopy and confocal microscopy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6842488/
https://www.ncbi.nlm.nih.gov/pubmed/31706282
http://dx.doi.org/10.1186/s12885-019-6226-8
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