Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report

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Gorlin-Goltz syndrome or basal cell nevi syndrome is an ectodermal neoplasia of autosomal dominant inheritance. It is a multisystem disease with a prevalence of 1 case per 57 000 to 150 000 people. It predominates in patients between the second and third decade of life, with a predilection for the m...

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Autores: Vinitzky Brener , Ilan, Carrasco Rueda, Carlos Alberto, Robledo Blancas, Julio César, Torres Hernández, Emmanuel
Formato: artículo
Fecha de Publicación:2024
Institución:Universidad de San Martín de Porres
Repositorio:Revistas - Universidad de San Martín de Porres
Lenguaje:español
OAI Identifier:oai:revistas.usmp.edu.pe:article/2774
Enlace del recurso:https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774
Nivel de acceso:acceso abierto
Materia:Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
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network_name_str Revistas - Universidad de San Martín de Porres
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dc.title.none.fl_str_mv Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
Manejo quirúrgico de queratoquiste odontogénico asociado a síndrome de Gorlin-Goltz. Reporte de un caso
title Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
spellingShingle Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
Vinitzky Brener , Ilan
Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
title_short Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
title_full Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
title_fullStr Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
title_full_unstemmed Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
title_sort Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case report
dc.creator.none.fl_str_mv Vinitzky Brener , Ilan
Carrasco Rueda, Carlos Alberto
Robledo Blancas, Julio César
Torres Hernández, Emmanuel
author Vinitzky Brener , Ilan
author_facet Vinitzky Brener , Ilan
Carrasco Rueda, Carlos Alberto
Robledo Blancas, Julio César
Torres Hernández, Emmanuel
author_role author
author2 Carrasco Rueda, Carlos Alberto
Robledo Blancas, Julio César
Torres Hernández, Emmanuel
author2_role author
author
author
dc.subject.none.fl_str_mv Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
topic Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
Síndrome de Gorlin-Goltz; Quistes odontogénicos; Odontología
description Gorlin-Goltz syndrome or basal cell nevi syndrome is an ectodermal neoplasia of autosomal dominant inheritance. It is a multisystem disease with a prevalence of 1 case per 57 000 to 150 000 people. It predominates in patients between the second and third decade of life, with a predilection for the male sex., Iit’s characterized by the presence of multiple basal cell nevus carcinomas, development of odontogenic keratocystic and palmo-plantar pits or dimples and calcification of the falx brain. Odontogenic keratocysts (OKC) occur in more than 80% of cases of patients with Gorlin-Goltz syndrome (GGS). OKC can present as the first sign of GGS. Approximately 65% of cases affect the mandible, with high frequency in the molar and ramus region. A clinical case is presented of a 35-year-old male patient with a current condition of missing teeth. Physical examination revealed syndromic facies. Orthopantomography is requested, observing multiple radiolucent areas of various sizes as well as retained dental organs, so vacuum puncture and incisional biopsy were taken.; Histopathological result: odontogenic keratocyst and suspicion of GGS because the patient meets the major and minor criteria; complementary studies were requested to confirm the diagnosis. Enucleation of cystic lesions with peripheral ostectomy, extraction of retained and excision of the skin lesion was performed under general anesthesia. After one year, the healing process and bone regeneration was observed without signs of recurrence. The patient was kept under control and monitored by our service with annual appointments.  
publishDate 2024
dc.date.none.fl_str_mv 2024-01-31
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dc.identifier.none.fl_str_mv https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774
10.24265/kiru.2024.v21n1.04
url https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774
identifier_str_mv 10.24265/kiru.2024.v21n1.04
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language spa
dc.relation.none.fl_str_mv https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774/3798
https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774/3799
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by/4.0
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dc.publisher.none.fl_str_mv Universidad de San Martín de Porres, Facultad de Odontología.
publisher.none.fl_str_mv Universidad de San Martín de Porres, Facultad de Odontología.
dc.source.none.fl_str_mv KIRU ; Vol. 21 No. 1 (2024): KIRU (ENE-MAR); 28-34
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spelling Surgical management of odontogenic keratocyst associated with Gorlin-Goltz syndrome.Case reportManejo quirúrgico de queratoquiste odontogénico asociado a síndrome de Gorlin-Goltz. Reporte de un casoVinitzky Brener , IlanCarrasco Rueda, Carlos AlbertoRobledo Blancas, Julio CésarTorres Hernández, EmmanuelSíndrome de Gorlin-Goltz; Quistes odontogénicos; OdontologíaSíndrome de Gorlin-Goltz; Quistes odontogénicos; OdontologíaGorlin-Goltz syndrome or basal cell nevi syndrome is an ectodermal neoplasia of autosomal dominant inheritance. It is a multisystem disease with a prevalence of 1 case per 57 000 to 150 000 people. It predominates in patients between the second and third decade of life, with a predilection for the male sex., Iit’s characterized by the presence of multiple basal cell nevus carcinomas, development of odontogenic keratocystic and palmo-plantar pits or dimples and calcification of the falx brain. Odontogenic keratocysts (OKC) occur in more than 80% of cases of patients with Gorlin-Goltz syndrome (GGS). OKC can present as the first sign of GGS. Approximately 65% of cases affect the mandible, with high frequency in the molar and ramus region. A clinical case is presented of a 35-year-old male patient with a current condition of missing teeth. Physical examination revealed syndromic facies. Orthopantomography is requested, observing multiple radiolucent areas of various sizes as well as retained dental organs, so vacuum puncture and incisional biopsy were taken.; Histopathological result: odontogenic keratocyst and suspicion of GGS because the patient meets the major and minor criteria; complementary studies were requested to confirm the diagnosis. Enucleation of cystic lesions with peripheral ostectomy, extraction of retained and excision of the skin lesion was performed under general anesthesia. After one year, the healing process and bone regeneration was observed without signs of recurrence. The patient was kept under control and monitored by our service with annual appointments.  EI síndrome de Gorlin-Goltz o síndrome de nevos basocelulares es una neoplasia ectodérmica de herencia autosómica dominante. Es una enfermedad multisistémica con una prevalencia de 1 caso por cada 57 000 a 150 000 personas. Predomina en pacientes entre la segunda y tercera década de vida, con predilección por el sexo masculino, se caracteriza por la presencia de múltiples carcinomas nevos basocelulares, desarrollo de queratoquistes odontogénicos y “pits” u hoyuelos palmo-plantares y calcificación de la hoz del cerebro. Los queratoquistes odontogénicos (QQO’s) ocurren en más del 80% de los casos de pacientes con síndrome de Gorlin-Goltz (SGG). Los QQO’s pueden presentarse como el primer signo de SGG. Aproximadamente en el 65% de los casos afecta la mandíbula, con alta frecuencia en la región de molares y rama. Se presenta caso clínico de un paciente masculino de 35 años con padecimiento actual de ausencia de piezas dentales, a la exploración física se observa facies sindrómicas. Se solicita ortopantomografía observando múltiples zonas radiolúcidas de diversos tamaños, así como órganos dentarios retenidos, se realiza punción aspiradora y toma de biopsia incisional; resultado histopatológico queratoquiste odontogénico y sospecha de SGG debido a que el paciente cumple con los criterios mayores y menores; se solicitan más estudios complementarios que confirman el diagnóstico. Se realiza enucleación de lesiones quísticas con ostectomía periférica y extracción de órganos dentarios retenidos. Al año se observa adecuado proceso de cicatrización y regeneración ósea sin datos de recidiva. El paciente se mantiene en control y seguimiento por nuestro servicio con citas anuales.Universidad de San Martín de Porres, Facultad de Odontología.2024-01-31info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/xmlhttps://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/277410.24265/kiru.2024.v21n1.04KIRU ; Vol. 21 No. 1 (2024): KIRU (ENE-MAR); 28-34 KIRU ISSN electrónico 2410-2717 ISSN Impreso 1812 - 7886; Vol. 21 Núm. 1 (2024): KIRU (ENE-MAR); 28-342410-27171812-7886reponame:Revistas - Universidad de San Martín de Porresinstname:Universidad de San Martín de Porresinstacron:USMPspahttps://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774/3798https://portalrevistas.aulavirtualusmp.pe/index.php/Rev-Kiru0/article/view/2774/3799Derechos de autor 2024 Ilan Vinitzky Brener , Carlos Alberto Carrasco Rueda , Julio César Robledo Blancas , Emmanuel Torres Hernández https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:revistas.usmp.edu.pe:article/27742025-03-06T15:36:24Z
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