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Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review
A subset of patients with Lynch Syndrome demonstrates cutaneous manifestations of the disorder. Characterization of these Lynch-related skin lesions could help in early recognition of patients with Lynch Syndrome. A broad search of the literature on OVID Medline and Embase was carried out to capture...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020322/ https://www.ncbi.nlm.nih.gov/pubmed/36418753 http://dx.doi.org/10.1007/s10689-022-00319-8 |
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author | Aziz, Shahram O’Sullivan, Hazel Heelan, Kara Alam, Afrina McVeigh, Terri P. |
author_facet | Aziz, Shahram O’Sullivan, Hazel Heelan, Kara Alam, Afrina McVeigh, Terri P. |
author_sort | Aziz, Shahram |
collection | PubMed |
description | A subset of patients with Lynch Syndrome demonstrates cutaneous manifestations of the disorder. Characterization of these Lynch-related skin lesions could help in early recognition of patients with Lynch Syndrome. A broad search of the literature on OVID Medline and Embase was carried out to capture papers reporting cutaneous manifestations in Lynch Syndrome patients. The results were uploaded into Mendeley reference management software. The PRISMA workflow was used in the literature selection process. In this systematic review, data were collected from 961 cases from 413 studies, including 380 molecularly confirmed Lynch Syndrome cases. The main skin lesions were: Sebaceous adenomas (43%), sebaceous carcinomas (27%), keratoacanthomas (16%), sebaceomas (13%), squamous cell carcinomas (23%), and basal cell carcinomas (10%). MSH2 variants were the most common underlying genotype (72%). Assessment of mismatch repair by immunohistochemistry, microsatellite instability analysis, or both were performed on 328 skin lesions from 220 (58%) molecularly confirmed cases. In those skin lesions, 95% of Immunohistochemistry and 90% of the microsatellite instability test results were concordant with the underlying genotype. Sebaceous skin lesions are well-recognised phenotypic features of Lynch Syndrome. Our results show that squamous and basal cell carcinomas are relatively common in patients with Lynch syndrome; however, available evidence cannot confirm that Lynch syndrome is causal. Immunohistochemistry and/or microsatellite instability testing of skin tumours in patients with a family history of Lynch Syndrome-associated cancers may be a useful approach in identifying patients requiring referral to Clinical Genetics and/or consideration of germline genetic testing for Lynch Syndrome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10689-022-00319-8. |
format | Online Article Text |
id | pubmed-10020322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-100203222023-03-18 Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review Aziz, Shahram O’Sullivan, Hazel Heelan, Kara Alam, Afrina McVeigh, Terri P. Fam Cancer Review A subset of patients with Lynch Syndrome demonstrates cutaneous manifestations of the disorder. Characterization of these Lynch-related skin lesions could help in early recognition of patients with Lynch Syndrome. A broad search of the literature on OVID Medline and Embase was carried out to capture papers reporting cutaneous manifestations in Lynch Syndrome patients. The results were uploaded into Mendeley reference management software. The PRISMA workflow was used in the literature selection process. In this systematic review, data were collected from 961 cases from 413 studies, including 380 molecularly confirmed Lynch Syndrome cases. The main skin lesions were: Sebaceous adenomas (43%), sebaceous carcinomas (27%), keratoacanthomas (16%), sebaceomas (13%), squamous cell carcinomas (23%), and basal cell carcinomas (10%). MSH2 variants were the most common underlying genotype (72%). Assessment of mismatch repair by immunohistochemistry, microsatellite instability analysis, or both were performed on 328 skin lesions from 220 (58%) molecularly confirmed cases. In those skin lesions, 95% of Immunohistochemistry and 90% of the microsatellite instability test results were concordant with the underlying genotype. Sebaceous skin lesions are well-recognised phenotypic features of Lynch Syndrome. Our results show that squamous and basal cell carcinomas are relatively common in patients with Lynch syndrome; however, available evidence cannot confirm that Lynch syndrome is causal. Immunohistochemistry and/or microsatellite instability testing of skin tumours in patients with a family history of Lynch Syndrome-associated cancers may be a useful approach in identifying patients requiring referral to Clinical Genetics and/or consideration of germline genetic testing for Lynch Syndrome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10689-022-00319-8. Springer Netherlands 2022-11-23 2023 /pmc/articles/PMC10020322/ /pubmed/36418753 http://dx.doi.org/10.1007/s10689-022-00319-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Aziz, Shahram O’Sullivan, Hazel Heelan, Kara Alam, Afrina McVeigh, Terri P. Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title | Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title_full | Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title_fullStr | Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title_full_unstemmed | Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title_short | Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
title_sort | characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020322/ https://www.ncbi.nlm.nih.gov/pubmed/36418753 http://dx.doi.org/10.1007/s10689-022-00319-8 |
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