Atypical thyroid manifestation in Cowden disease: a case report and literature review

Atypical thyroid manifestation in Cowden disease: a case report and literature review

BackgroundCowden syndrome (CS) is a complex and rare hereditary disorder characterized by a high risk of developing both benign and malignant tumors. Germline variants in the PTEN gene lead to this autosomal dominant syndrome, which predisposes individuals to lesions of the skin and mucous membranes...

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Bibliographic Details
Main Authors: Marion Garcia, Isabelle Oliver Petit, Camille Franchet, Olivier Abbo, Audrey Cartault, Frédérique Savagner
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Pediatrics
Subjects:
Cowden syndrome
childhood
thyroid pathologies
PTEN variant
hyperfunctioning nodule
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2025.1499664/full
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