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Challenges in the management of a patient with Cowden syndrome: case report and literature review
We would like to present a patient with a classical phenotype of a rare disorder - Cowden syndrome, its diagnostics and management challenges. A breast surgeon has to be aware of this rare condition when treating a patient with breast manifestations of Cowden syndrome and has to refer the patient to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350443/ https://www.ncbi.nlm.nih.gov/pubmed/22503188 http://dx.doi.org/10.1186/1897-4287-10-5 |
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author | Melbārde-Gorkuša, Inga Irmejs, Arvīds Bērziņa, Dace Štrumfa, Ilze Āboliņš, Arnis Gardovskis, Andris Subatniece, Signe Trofimovičs, Genādijs Gardovskis, Jānis Miklaševičs, Edvīns |
author_facet | Melbārde-Gorkuša, Inga Irmejs, Arvīds Bērziņa, Dace Štrumfa, Ilze Āboliņš, Arnis Gardovskis, Andris Subatniece, Signe Trofimovičs, Genādijs Gardovskis, Jānis Miklaševičs, Edvīns |
author_sort | Melbārde-Gorkuša, Inga |
collection | PubMed |
description | We would like to present a patient with a classical phenotype of a rare disorder - Cowden syndrome, its diagnostics and management challenges. A breast surgeon has to be aware of this rare condition when treating a patient with breast manifestations of Cowden syndrome and has to refer the patient to a clinical geneticist for further evaluation. Sequencing of the PTEN gene showed the Asp24Gly mutation. According to the latest literature data, the lifetime risk of breast cancer for Cowden syndrome patients is 81% and surgery is a justified option to reduce the risk of breast cancer. Bilateral risk-reducing mastectomy with immediate reconstruction was performed to eliminate further risk of breast cancer. 3 years after the risk-reducing breast surgery the patient is satisfied with the outcome. This is to our best knowledge the first reported Cowden syndrome case with follow-up data after risk-reducing measures have been taken. |
format | Online Article Text |
id | pubmed-3350443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33504432012-05-12 Challenges in the management of a patient with Cowden syndrome: case report and literature review Melbārde-Gorkuša, Inga Irmejs, Arvīds Bērziņa, Dace Štrumfa, Ilze Āboliņš, Arnis Gardovskis, Andris Subatniece, Signe Trofimovičs, Genādijs Gardovskis, Jānis Miklaševičs, Edvīns Hered Cancer Clin Pract Case Report We would like to present a patient with a classical phenotype of a rare disorder - Cowden syndrome, its diagnostics and management challenges. A breast surgeon has to be aware of this rare condition when treating a patient with breast manifestations of Cowden syndrome and has to refer the patient to a clinical geneticist for further evaluation. Sequencing of the PTEN gene showed the Asp24Gly mutation. According to the latest literature data, the lifetime risk of breast cancer for Cowden syndrome patients is 81% and surgery is a justified option to reduce the risk of breast cancer. Bilateral risk-reducing mastectomy with immediate reconstruction was performed to eliminate further risk of breast cancer. 3 years after the risk-reducing breast surgery the patient is satisfied with the outcome. This is to our best knowledge the first reported Cowden syndrome case with follow-up data after risk-reducing measures have been taken. BioMed Central 2012-04-14 /pmc/articles/PMC3350443/ /pubmed/22503188 http://dx.doi.org/10.1186/1897-4287-10-5 Text en Copyright ©2012 Melbārde-Gorkuša et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Melbārde-Gorkuša, Inga Irmejs, Arvīds Bērziņa, Dace Štrumfa, Ilze Āboliņš, Arnis Gardovskis, Andris Subatniece, Signe Trofimovičs, Genādijs Gardovskis, Jānis Miklaševičs, Edvīns Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title | Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title_full | Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title_fullStr | Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title_full_unstemmed | Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title_short | Challenges in the management of a patient with Cowden syndrome: case report and literature review |
title_sort | challenges in the management of a patient with cowden syndrome: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350443/ https://www.ncbi.nlm.nih.gov/pubmed/22503188 http://dx.doi.org/10.1186/1897-4287-10-5 |
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