Challenges in the management of a patient with Cowden syndrome: case report and literature review

<p>Abstract</p> <p>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 syn...

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Bibliographic Details
Main Authors: Melbārde-Gorkuša Inga, Irmejs Arvīds, Bērziņa Dace, Štrumfa Ilze, Āboliņš Arnis, Gardovskis Andris, Subatniece Signe, Trofimovičs Genādijs, Gardovskis Jānis, Miklaševičs Edvīns
Format: Article
Language:English
Published: BMC 2012-04-01
Series:Hereditary Cancer in Clinical Practice
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Online Access:http://www.hccpjournal.com/content/10/1/5
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Summary:<p>Abstract</p> <p>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 <it>PTEN </it>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.</p>
ISSN:1897-4287