Search engine for discovering works of Art, research articles, and books related to Art and Culture
Javascript must be enabled to continue!
Queratoquiste odontogénico en síndrome de Gorlin-Goltz
View through CrossRef
Introduction: Gorlin-Goltz syndrome (GGS) is a genetic disorder characterized by basal cell carcinomas, odontogenic keratocysts (OCK) and skeletal anomalies. Clinical case: An 11-year-old male who presents with a painless tumor in the left maxillary region, with a family history of GGS. Physical examination revealed a tumor measuring 3 cm in diameter. The CT scan shows a tumor occupying the maxillary sinus. Endoscopic sinonasal surgery was performed for biopsy, resulting in an OKC. Discussion: GGS is a rare entity; within its clinical presentation are OKCs, which are difficult to diagnose and require aggressive surgical management to avoid recurrence. Conclusion: Early disease detection makes it possible to analyze other clinical manifestations, such as OKC early.
Asociacion Colombiana de Otorrinolaringologia
Title: Queratoquiste odontogénico en síndrome de Gorlin-Goltz
Description:
Introduction: Gorlin-Goltz syndrome (GGS) is a genetic disorder characterized by basal cell carcinomas, odontogenic keratocysts (OCK) and skeletal anomalies.
Clinical case: An 11-year-old male who presents with a painless tumor in the left maxillary region, with a family history of GGS.
Physical examination revealed a tumor measuring 3 cm in diameter.
The CT scan shows a tumor occupying the maxillary sinus.
Endoscopic sinonasal surgery was performed for biopsy, resulting in an OKC.
Discussion: GGS is a rare entity; within its clinical presentation are OKCs, which are difficult to diagnose and require aggressive surgical management to avoid recurrence.
Conclusion: Early disease detection makes it possible to analyze other clinical manifestations, such as OKC early.
Related Results
Fibromixoma odontogênico associado a um cisto odontogênico mimetizando sarcoma fibromixóide de baixo grau
Fibromixoma odontogênico associado a um cisto odontogênico mimetizando sarcoma fibromixóide de baixo grau
Introdução: O fibromixoma odontogênico é um tumor benigno raro, variante do mixoma odontogênico, caracterizado histologicamente por uma quantidade excessiva de fibras colágenas. Ap...
CISTO ODONTOGÊNICO CALCIFICANTE: RELATO DE CASO DE CISTO DE GORLIN UTILIZANDO TÉCNICAS DE MARSUPIALIZAÇÃO E ENUCLEAÇÃO
CISTO ODONTOGÊNICO CALCIFICANTE: RELATO DE CASO DE CISTO DE GORLIN UTILIZANDO TÉCNICAS DE MARSUPIALIZAÇÃO E ENUCLEAÇÃO
O Cisto de Gorlin, também denominado Cisto Odontogênico Calcificante, é uma lesão incomum, que teve divergências em sua classificação. Anteriormente em 2005 era denominado Tumor C...
Gorlin Goltz Syndrome: A Disease in Disguise
Gorlin Goltz Syndrome: A Disease in Disguise
Gorlin Goltz syndrome also known as nevoid basal cell carcinoma is an autosomal dominant inherited disorder caused due to mutation in patched (PTCH) tumor suppressor gene present i...
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
: Focal dermal hypoplasia, popularly known as the goltz syndrome, is an extremely rare multisystem disorder mainly involving the skin, skeletal system, and eyes. Being an X-linked ...
Queratoquiste odontogenico recurrente en paciente con sindrome de Gorlin-Goltz
Queratoquiste odontogenico recurrente en paciente con sindrome de Gorlin-Goltz
El Síndrome de Gorlin-Goltz (SGG) es un desorden autosómico dominante, se caracteriza por presentar anoma- lías esqueléticas, Queratoquistes Odontogénicos (QQOs) múltiples y carcin...
GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW
GOLTZ GORLIN SYNDROME- A CASE REPORT WITH OVERVIEW
Goltz Gorlin syndrome (GGS) is an multisystemic disease with an autosomal dominant disorder, with complete variance, though irregular cases have been described. This article includ...
Síndrome Gorlin-Goltz: relato de caso
Síndrome Gorlin-Goltz: relato de caso
Síndrome Gorlin-Goltz (SGG) é uma desordem rara autossômica dominante. Apesar de hereditária, há casos de mutação espontânea. Caracteriza-se pela predisposição cancerígena e várias...
Proservação pós-operatória de paciente com Síndrome de Gorlin-Goltz – relato de caso
Proservação pós-operatória de paciente com Síndrome de Gorlin-Goltz – relato de caso
Introdução: A Síndrome de Gorlin-Goltz, também conhecida como Síndrome do Carcinoma Basocelular Nevoide, é um transtorno hereditário autossômico dominante que se caracteriza pela p...