Late diagnosis and oral rehabilitation in a patient with Cowden syndrome: case report

Autores/as

DOI:

https://doi.org/10.5327/2525-5711.416

Palabras clave:

Cowden Syndrome, PTEN Tumor Suppressor Gene, Oral Manifestations, Case Report, Oral Rehabilitation

Resumen

Cowden syndrome is a rare autosomal dominant disorder associated with germline mutations in the PTEN gene and characterized by multiple hamartomas and an increased risk of malignancy. A 64-year-old woman was referred for evaluation of papillomatous lesions in the oral cavity. Clinical examination revealed verrucous lesions, macrocephaly, acral keratoses, and facial trichilemmomas. Complementary examinations showed benign breast nodules and gastrointestinal polyposis without malignant transformation. Based on clinical, histopathological, and imaging findings, a diagnosis of Cowden syndrome was established according to the criteria of the International Cowden Syndrome Consortium. The patient underwent surgical excision of the oral papillomatous lesions followed by prosthetic rehabilitation with complete removable dentures, which restored function and aesthetics. This report emphasizes the essential role of dentists in the recognition of Cowden syndrome and in the multidisciplinary management required for affected patients.

Citas

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Publicado

2026-03-27

Cómo citar

1.
Miranda de Oliveira Abdalla G, Maria Cotta L, Miranda Pernambuco C, Goulart Silvério A, Ervolino de Oliveira C, Haddad MF, et al. Late diagnosis and oral rehabilitation in a patient with Cowden syndrome: case report. J Oral Diagn [Internet]. 27 de marzo de 2026 [citado 17 de abril de 2026];11. Disponible en: https://jordi.com.br/revista/article/view/416

Número

Sección

Case Report