NUMERO: #20230470

Título: GORLIN-GOLTZ SYNDROME - CLINICAL CASE REPORT

Nome do Apresentador: Bruna Carvalho Lopez Moreno

Categoria do Trabalho: Painel de caso clínico (PCC)

Área Temática: Estomatologia

Resumo: Gorlin-Goltz syndrome is an autosomal dominant inherited disease characterized by the occurrence of cutaneous basal cell carcinomas, odontogenic keratocysts, intracranial calcifications and rib abnormalities, among other changes. A 13-year-old male patient came to a Bucomaxilofacial Surgery Service with his father complaining of swelling on the right hemiface. The parent reported that his son had been diagnosed as having Gorlin-Goltz syndrome, with a medical history of basal cell carcinoma, bifid ribs, and intracranial calcification. Facial asymmetry was observed on the right side in the molar region. A slight palatal swelling with hardened consistency was also observed. Imaging findings showed radiolucent, unilocular lesions, well delimited. Incisional biopsy was performed in the maxilla and excisional biopsy in the bilateral retromolar region. The anatomopathological diagnosis was Odontogenic Keratocyst. Enucleation of the cysts was performed associated with cryotherapy with liquid nitrogen. In the postoperative period of 3 years, there was no recurrence of the lesion.

Autor 1:  Bruna Carvalho Lopez Moreno

E-mail 1:  [email protected]

Autor 2:   Daniela Gomes Castro dos Santos

E-mail 2:  [email protected]

Autor 3 :  Matheus Gonçalves Ferreira Leal

E-mail 3:  [email protected]

Autor 4:  Antônio Lucindo Pinto de Campos Sobrinho

E-mail 4:  [email protected]

Autor 5:  Silvia Regina de Almeida Reis

E-mail 5:  [email protected]

Autor 6:  Alena Ribeiro Alves Peixoto Medrado

E-mail 6:  [email protected]