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Hereditary gingival fibromatosis and its management: 2-year follow-up

Hereditary gingival fibromatosis (HGF) is a rare hereditary condition characterised by slow, progressive, nonhemorrhagic, fibrous enlargement of gingiva caused by increase in sub-mucosal connective tissue component. This paper presents a case report of a 14-year-old male suffering from HGF with posi...

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Autores principales: Tripathi, Amitandra Kumar, Upadhaya, Vinod, Kumar, Vivek, Saimbi, C. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229776/
https://www.ncbi.nlm.nih.gov/pubmed/25395783
http://dx.doi.org/10.4103/0976-237X.142835
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author Tripathi, Amitandra Kumar
Upadhaya, Vinod
Kumar, Vivek
Saimbi, C. S.
author_facet Tripathi, Amitandra Kumar
Upadhaya, Vinod
Kumar, Vivek
Saimbi, C. S.
author_sort Tripathi, Amitandra Kumar
collection PubMed
description Hereditary gingival fibromatosis (HGF) is a rare hereditary condition characterised by slow, progressive, nonhemorrhagic, fibrous enlargement of gingiva caused by increase in sub-mucosal connective tissue component. This paper presents a case report of a 14-year-old male suffering from HGF with positive family history. After through clinical examination, routine blood investigation was advised. All the parameters were within normal physiological limits. Surgical excision of enlarged gingival mass was planned after meticulous scaling and root planning. Patient was recalled 1-week after surgery. Postoperative healing was good and desired crown lengthening was achieved with significant improvement in speech and masticatory problems. There was no recurrence of the disease even after 2 years follow-up.
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spelling pubmed-42297762014-11-13 Hereditary gingival fibromatosis and its management: 2-year follow-up Tripathi, Amitandra Kumar Upadhaya, Vinod Kumar, Vivek Saimbi, C. S. Contemp Clin Dent Case Report Hereditary gingival fibromatosis (HGF) is a rare hereditary condition characterised by slow, progressive, nonhemorrhagic, fibrous enlargement of gingiva caused by increase in sub-mucosal connective tissue component. This paper presents a case report of a 14-year-old male suffering from HGF with positive family history. After through clinical examination, routine blood investigation was advised. All the parameters were within normal physiological limits. Surgical excision of enlarged gingival mass was planned after meticulous scaling and root planning. Patient was recalled 1-week after surgery. Postoperative healing was good and desired crown lengthening was achieved with significant improvement in speech and masticatory problems. There was no recurrence of the disease even after 2 years follow-up. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4229776/ /pubmed/25395783 http://dx.doi.org/10.4103/0976-237X.142835 Text en Copyright: © Contemporary Clinical Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tripathi, Amitandra Kumar
Upadhaya, Vinod
Kumar, Vivek
Saimbi, C. S.
Hereditary gingival fibromatosis and its management: 2-year follow-up
title Hereditary gingival fibromatosis and its management: 2-year follow-up
title_full Hereditary gingival fibromatosis and its management: 2-year follow-up
title_fullStr Hereditary gingival fibromatosis and its management: 2-year follow-up
title_full_unstemmed Hereditary gingival fibromatosis and its management: 2-year follow-up
title_short Hereditary gingival fibromatosis and its management: 2-year follow-up
title_sort hereditary gingival fibromatosis and its management: 2-year follow-up
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229776/
https://www.ncbi.nlm.nih.gov/pubmed/25395783
http://dx.doi.org/10.4103/0976-237X.142835
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