Cargando…

Hereditary gingival fibromatosis: Characteristics and treatment approach

Hereditary gingival fibromatosis (HGF) is a rare disorder characterized by a benign, non-hemorrhagic, fibrous gingival overgrowth that can appear in isolation or as part of a syndrome. Clinically, a pink gingiva with marked stippling can be seen to cover almost all the tooth, in many cases preventin...

Descripción completa

Detalles Bibliográficos
Autores principales: Almiñana-Pastor, Pedro J., Buitrago-Vera, Pedro J., Alpiste-Illueca, Francisco M., Catalá-Pizarro, Montserrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410686/
https://www.ncbi.nlm.nih.gov/pubmed/28469831
http://dx.doi.org/10.4317/jced.53644
_version_ 1783232732673867776
author Almiñana-Pastor, Pedro J.
Buitrago-Vera, Pedro J.
Alpiste-Illueca, Francisco M.
Catalá-Pizarro, Montserrat
author_facet Almiñana-Pastor, Pedro J.
Buitrago-Vera, Pedro J.
Alpiste-Illueca, Francisco M.
Catalá-Pizarro, Montserrat
author_sort Almiñana-Pastor, Pedro J.
collection PubMed
description Hereditary gingival fibromatosis (HGF) is a rare disorder characterized by a benign, non-hemorrhagic, fibrous gingival overgrowth that can appear in isolation or as part of a syndrome. Clinically, a pink gingiva with marked stippling can be seen to cover almost all the tooth, in many cases preventing eruption. HGF usually begins during the transition from primary to permanent teeth, giving rise to a condition that can have negative psychological effects at that age. As it does not resolve spontaneously, the treatment of choice is gingivectomy, which can be performed with an internal or external bevel incision, depending on each case and bearing in mind the changes that will take place at the dentogingival junction (DGJ). This paper describes clinical aspects and treatment in two eight-year-old boys with HGF, considering different facets of the surgical approach with conscious sedation in young children. Key words:Hereditary gingival fibromatosis, gingivectomy, internal bevel incision, external bevel incision, gingival overgrowth.
format Online
Article
Text
id pubmed-5410686
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medicina Oral S.L.
record_format MEDLINE/PubMed
spelling pubmed-54106862017-05-03 Hereditary gingival fibromatosis: Characteristics and treatment approach Almiñana-Pastor, Pedro J. Buitrago-Vera, Pedro J. Alpiste-Illueca, Francisco M. Catalá-Pizarro, Montserrat J Clin Exp Dent Case Report Hereditary gingival fibromatosis (HGF) is a rare disorder characterized by a benign, non-hemorrhagic, fibrous gingival overgrowth that can appear in isolation or as part of a syndrome. Clinically, a pink gingiva with marked stippling can be seen to cover almost all the tooth, in many cases preventing eruption. HGF usually begins during the transition from primary to permanent teeth, giving rise to a condition that can have negative psychological effects at that age. As it does not resolve spontaneously, the treatment of choice is gingivectomy, which can be performed with an internal or external bevel incision, depending on each case and bearing in mind the changes that will take place at the dentogingival junction (DGJ). This paper describes clinical aspects and treatment in two eight-year-old boys with HGF, considering different facets of the surgical approach with conscious sedation in young children. Key words:Hereditary gingival fibromatosis, gingivectomy, internal bevel incision, external bevel incision, gingival overgrowth. Medicina Oral S.L. 2017-04-01 /pmc/articles/PMC5410686/ /pubmed/28469831 http://dx.doi.org/10.4317/jced.53644 Text en Copyright: © 2017 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Almiñana-Pastor, Pedro J.
Buitrago-Vera, Pedro J.
Alpiste-Illueca, Francisco M.
Catalá-Pizarro, Montserrat
Hereditary gingival fibromatosis: Characteristics and treatment approach
title Hereditary gingival fibromatosis: Characteristics and treatment approach
title_full Hereditary gingival fibromatosis: Characteristics and treatment approach
title_fullStr Hereditary gingival fibromatosis: Characteristics and treatment approach
title_full_unstemmed Hereditary gingival fibromatosis: Characteristics and treatment approach
title_short Hereditary gingival fibromatosis: Characteristics and treatment approach
title_sort hereditary gingival fibromatosis: characteristics and treatment approach
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410686/
https://www.ncbi.nlm.nih.gov/pubmed/28469831
http://dx.doi.org/10.4317/jced.53644
work_keys_str_mv AT alminanapastorpedroj hereditarygingivalfibromatosischaracteristicsandtreatmentapproach
AT buitragoverapedroj hereditarygingivalfibromatosischaracteristicsandtreatmentapproach
AT alpisteilluecafranciscom hereditarygingivalfibromatosischaracteristicsandtreatmentapproach
AT catalapizarromontserrat hereditarygingivalfibromatosischaracteristicsandtreatmentapproach