Hereditary gingival fibromatosis - a case report and management using a novel surgical technique
RSBO (Impr.)
; 8(4): 453-458, Oct.-Dec. 2011. ilus
Article
em En
| LILACS
| ID: lil-744223
Biblioteca responsável:
BR97.1
ABSTRACT
Introduction:
Hereditary gingival fibromatosis (HGF) is a rare condition presenting varied degrees of gingival enlargement. HGF can present as an isolated entity or as part of a syndrome. Current literatures report a defect in the Son of sevenless-1 gene (SOS-1) on chromosome 2p21-p22 (HGF1) as a possible cause of this condition. Case report A case of a 16-year-old female is reported who presented generalized extensive gingival overgrowth, involving the maxillary and mandibular arches covering almost two thirds to three quarters of all teeth. Diagnosis of HGF was substantiated by the patient's clinical features, family history and histopathological examination. Treatment was excision of the gingival tissue by a modified gingivectomy technique with both manual instrumentation and electrosurgery. The postoperative course was uneventful and the patient's aesthetic concerns were addressed. Post-surgical follow-up after 18 months demonstrated no recurrence.Conclusion:
Hereditary gingival fibromatosis stands apart from other gingival enlargements in the varied treatment options available and the nature of recurrence post treatment. There is no consensus among authors related to the mode of treatment. Here, in this present case report we highlight a novel surgical technique to deal with the extensive nature of enlargement seen in HGF cases.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
LILACS
Tipo de estudo:
Guideline
Idioma:
En
Revista:
RSBO (Impr.)
Assunto da revista:
ODONTOLOGIA
Ano de publicação:
2011
Tipo de documento:
Article
País de afiliação:
Índia
País de publicação:
Brasil