Clinical observation reveals cowden syndrome in a patient with papillary thyroid carcinoma, highlighting early diagnosis importance.
Cowden syndrome is a rare genetic disorder, often linked to PTEN gene mutations, characterized by a predisposition to various cancers. We report the case of a patient presenting with papillary thyroid carcinoma revealing the syndrome, highlighting the importance of early diagnosis and multidisciplinary management.
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K et al. (2026) studied this question.
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