NUMERO: #20240970

Título: DIAGNOSIS AND GENETIC CONSIDERATIONS IN GORLIN-GOLTZ SYNDROME: A CASE REPORT OF MULTIGENERATIONAL MANIFESTATION

Nome do Apresentador: Larissa Tinô de CARVALHO-SILVA

Categoria do Trabalho: Painel de caso clínico (PCC)

Área Temática: Estomatologia

Resumo: Male patient, 16 years old, presented with the chief complaint of swelling in the maxilla. The medical history was unremarkable, except for a paternal history of basal cell carcinoma. Extraoral examination showed facial asymmetry. Intraoral examination revealed a swelling covered by normal mucosa with hard consistency, in the left maxilla. Panoramic radiograph showed well-defined radiolucency causing displacement of canine and both premolars. An incisional biopsy diagnosed a keratocyst. Treatment consisted of marsupialization, followed by complete surgical excision and subsequent orthodontic approach. The patient was lost to follow-up and returned decades later with other jaw lesions. In addition, he had basal cell carcinomas and the diagnosis of Gorlin-Goltz syndrome. Accompanying him was his 10-year-old daughter, who also presented with increased volume in her left jaw and an incisional biopsy revealed a keratocyst. Both were referred for lesion removal. Genetic counseling was provided, and family was referred for multiprofessional follow-up.

Autor 1:  Larissa Tinô de CARVALHO-SILVA

E-mail 1:  [email protected]

Autor 2:   Ivan José CORREIA NETO

E-mail 2:  [email protected]

Autor 3 :  Brenda Corrêa SANTOS

E-mail 3:  [email protected]

Autor 4:  Alan Roger SANTOS-SILVA

E-mail 4:  [email protected]

Autor 5:  Pablo Agustin VARGAS

E-mail 5:  [email protected]

Autor 6:  Márcio Ajudarte LOPES

E-mail 6:  [email protected]