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Cowden Disease |
Credits: 1.25 Post-Assessment Questions: 10
Release Date: 5 Oct 2020
Expiration Date: 17 Jan 2022
Last Reviewed: 17 Jan 2021
Estimated Time To Finish: 75 Minutes
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Cowden disease, also known as Cowden syndrome or multiple hamartoma syndrome, is an uncommon autosomal dominant genodermatosis and is a member of the spectrum of disorders involving mutations in the phosphatase and tensin homolog gene. Cowden syndrome represents the most common phenotype associated with this spectrum and it is classically is characterized by multiple benign hamartomas that can occur in any organ. Patients with Cowden syndrome characteristically develop mucocutaneous lesions and macrocephaly. The majority of patients with Cowden syndrome develop a malignant neoplasm of the thyroid, endometrium, or breast. This activity describes the pathophysiology, evaluation, and management of Cowden syndrome and highlights the role of the interprofessional team in the care of affected patients.
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Authors: Craig Garofola, Zohaib Jamal
Editors: Gary Gross
Editors-In-Chief: Smita JhaSartaj SandhuVishnu Garla
Chief Medical Reviewer: Muhammad Hashmi
Nurse Planner/Reviewer/Editor: Lisa Haddad
Nurse Planner/Reviewer/Editor: Bernadette Makar
Nurse Planner/Reviewer/Editor: Dorothy Caputo
Pharmacy Planner/Reviewer/Editor: Mark Pellegrini
Physician Planner/Reviewer/Editor: Scott Dulebohn
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Quillen College of Medicine, East Tennessee State University designates this activity for a maximum of 1.25 AMA PRA Category 1 CreditsTM. Physicians should only claim credit commensurate with the extent of their participation in the activity.
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