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Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report
Idiopathic gingival fibromatosis is a genetic rare disorder, which is characterized by a progressive enlargement of the gingiva. Gingival enlargement is an overgrowth of the gingiva, which can be caused by various etiological factors such as poor oral hygiene, plaque accumulation, inadequate nutriti...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Jaypee Brothers Medical Publishers
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311769/ https://www.ncbi.nlm.nih.gov/pubmed/34326603 http://dx.doi.org/10.5005/jp-journals-10005-1933 |
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author | Kumari, Amrita Bansal, Malvika B Asrani, Karan H Yadav, Ashish |
author_facet | Kumari, Amrita Bansal, Malvika B Asrani, Karan H Yadav, Ashish |
author_sort | Kumari, Amrita |
collection | PubMed |
description | Idiopathic gingival fibromatosis is a genetic rare disorder, which is characterized by a progressive enlargement of the gingiva. Gingival enlargement is an overgrowth of the gingiva, which can be caused by various etiological factors such as poor oral hygiene, plaque accumulation, inadequate nutrition, hormonal stimulation, several blood dyscrasias, or long-term intake of certain drugs like phenytoin, nifedipine, or cyclosporine. A 14-year-old female patient reported to the Department of Periodontology, Mahatma Gandhi Dental College and Hospital, Jaipur, Rajasthan with her chief complaint of swollen gums in both upper and lower arches since 3 years, which was gradual in onset and increased in size since 4 months which covered almost half of the surface of each tooth. Also reported that 3 years ago, there was similar swelling for which surgical intervention in form of gingivectomy was carried out. The treatment plan for this case was followed by phase 1 therapy (scaling and root planing) and after completion of phase 1 therapy, the labial tissue from the mandibular anterior region was excised and sent for histopathological examination. Histopathological appearance revealed idiopathic gingival fibromatosis. Thereafter, the conventional gingivectomy under local anesthesia was performed to remove excess gingival overgrowth. How to cite this article: Kumari A, Bansal MB, Asrani KH, et al. Non-syndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report. Int J Clin Pediatr Dent 2021;14(1):158–160. |
format | Online Article Text |
id | pubmed-8311769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-83117692021-07-28 Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report Kumari, Amrita Bansal, Malvika B Asrani, Karan H Yadav, Ashish Int J Clin Pediatr Dent Case Report Idiopathic gingival fibromatosis is a genetic rare disorder, which is characterized by a progressive enlargement of the gingiva. Gingival enlargement is an overgrowth of the gingiva, which can be caused by various etiological factors such as poor oral hygiene, plaque accumulation, inadequate nutrition, hormonal stimulation, several blood dyscrasias, or long-term intake of certain drugs like phenytoin, nifedipine, or cyclosporine. A 14-year-old female patient reported to the Department of Periodontology, Mahatma Gandhi Dental College and Hospital, Jaipur, Rajasthan with her chief complaint of swollen gums in both upper and lower arches since 3 years, which was gradual in onset and increased in size since 4 months which covered almost half of the surface of each tooth. Also reported that 3 years ago, there was similar swelling for which surgical intervention in form of gingivectomy was carried out. The treatment plan for this case was followed by phase 1 therapy (scaling and root planing) and after completion of phase 1 therapy, the labial tissue from the mandibular anterior region was excised and sent for histopathological examination. Histopathological appearance revealed idiopathic gingival fibromatosis. Thereafter, the conventional gingivectomy under local anesthesia was performed to remove excess gingival overgrowth. How to cite this article: Kumari A, Bansal MB, Asrani KH, et al. Non-syndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report. Int J Clin Pediatr Dent 2021;14(1):158–160. Jaypee Brothers Medical Publishers 2021 /pmc/articles/PMC8311769/ /pubmed/34326603 http://dx.doi.org/10.5005/jp-journals-10005-1933 Text en Copyright © 2021; Jaypee Brothers Medical Publishers (P) Ltd. https://creativecommons.org/licenses/by-nc/4.0/© Jaypee Brothers Medical Publishers. 2021 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Kumari, Amrita Bansal, Malvika B Asrani, Karan H Yadav, Ashish Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title | Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title_full | Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title_fullStr | Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title_full_unstemmed | Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title_short | Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report |
title_sort | nonsyndromic with recurrent idiopathic gingival fibromatosis: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311769/ https://www.ncbi.nlm.nih.gov/pubmed/34326603 http://dx.doi.org/10.5005/jp-journals-10005-1933 |
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