Please use this identifier to cite or link to this item: 10.1186/1897-4287-10-5
Title: Challenges in the management of a patient with Cowden syndrome : Case report and literature review
Authors: Melbarde-Gorkuša, Inga
Irmejs, Arvids
Berziņa, Dace
Štrumfa, Ilze
Aboliņš, Arnis
Gardovskis, Andris
Subatniece, Signe
Trofimovičs, Genadijs
Gardovskis, Janis
Miklaševičs, Edvins
Hereditary Cancer Research Department
Keywords: Cancer;Cowden syndrome;PTEN;Risk-reducing mastectomy;3.1 Basic medicine;3.2 Clinical medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;Oncology;Genetics(clinical);SDG 3 - Good Health and Well-being
Issue Date: 14-Apr-2012
Citation: Melbarde-Gorkuša , I , Irmejs , A , Berziņa , D , Štrumfa , I , Aboliņš , A , Gardovskis , A , Subatniece , S , Trofimovičs , G , Gardovskis , J & Miklaševičs , E 2012 , ' Challenges in the management of a patient with Cowden syndrome : Case report and literature review ' , Hereditary cancer in clinical practice , vol. 10 , no. 1 , 5 . https://doi.org/10.1186/1897-4287-10-5 , https://doi.org/10.1186/1897-4287-10-5
Abstract: 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.
DOI: 10.1186/1897-4287-10-5
ISSN: 1731-2302
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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