Published April 10, 2022
| Version v1
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Aesthetic Management of Idiopathic Gingival Enlargement: A Case Report
Creators
- 1. Senior Resident
- 2. Professor & Head of Department
- 3. Professor
- 4. Senior Research Associate
- 5. PG Student
Description
Gingival enlargement is a common clinical condition caused by a number of reasons that includes inflammation, medications, systemic diseases and conditions etc. The balance between gingiva and clinical portion of teeth is lost resulting in poor aesthetics. Idiopathic gingival enlargement is a rare condition of undetermined cause characterized by progressive fibrous overgrowth of the gingival tissues. Gingivectomy is the treatment of choice which can be done by surgical excision using scalpels, electrocautery & electrosurgery, soft tissue lasers etc. This case report presents “aesthetic management of idiopathic gingival enlargement in a 17 year old male patient.”
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References
- Newman MG, Takei HH, Klokkevold PR, Carranza FA (2019). Newman and Carranza's Clinical Periodontology (13thed.). Philadelphia: Elsevier 2019; pp. 1523-1572.
- Ramer M, Marrone J, Stahl B, Burakoff R. Hereditary gingival fibromatosis: Identification, treatment, control. J Am Dent Assoc 1996;127:493-5.
- Bozzo L, Almedia OP, Scully C, Aldred MJ. Hereditary gingival fibromatosis: Report of an extensive four generation pedigree. Oral Surg Oral Med Oral Pathol 1998;86:304-7.
- Hart TC, Hart PS. Genetic studies of craniofacial anomalies: clinical implications and applications. OrthodCraniofac Res. 2009;12:212–220.
- Hart TC, Zhang Y, Gorry MC, et al. A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. Am J Hum Genet. 2002;70:943–954.
- Ye X, Shi L, Cheng Y, et al. A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3. Clin Genet. 2005;68:239–244.
- Zhang Y, Gorry MC, Hart PS, et al. Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-p21. Cytogenet Cell Genet. 2001;95:146– 152.
- Ramer M, Marrone J, Stahl B, Burakoff R. Hereditary gingival fibromatosis: Identification, treatment, control. J Am Dent Assoc 1996;127:493-5.
- Takagi M, Yamamoto H, Mega H, Hsieh KJ, Shioda S, Enomotos S. Heterogeneity in the gingival fibromatoses. Cancer 1991;68:2202-12.
- Wynne SE, Aldred MJ, Bartold PM. Hereditary gingival fibromatosis with hearing loss and supernumerary teeth-a new syndrome. J Periodontol 1995;66:75-9.
- Arora N, Vizo K, Bharti V. A Case Report of Idiopathic Gingival Enlargement with Tooth Repositioning after Surgical Therapy. Int J Oral Health Med Res 2016;3(4):72-74.
- Moss JP, Picton DCA. The causes of migration of teeth. In: Cook JT, ed. Transactions of the 3rd International Orthodontic Congress held in London, 13-18 August 1973. London: Crosby Lockwood Staples; 1975: 536-543.
- Picton DCA, Moss JP. The part played by the transseptalfibre system in experimental Approximal drift of the cheek teeth of monkeys. Arch Oral Biol 1973; 18: 669-680.