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Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas
BACKGROUND: Aggressive familial giant-cell granulomas of the jaws can be severely deforming. Surgical and nonsurgical treatments may be associated with multiple recurrences. Denosumab, a new generation antiresorptive drug, is an osteoclast inhibitor, which may be particularly useful to manage such p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327812/ https://www.ncbi.nlm.nih.gov/pubmed/30693243 http://dx.doi.org/10.4103/ams.ams_192_18 |
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author | Rytkönen, Eelis Ottavainen, Vuokko Rytkönen, Aleksi Uusitalo, Sanna Lehenkari, Petri Sándor, George K. |
author_facet | Rytkönen, Eelis Ottavainen, Vuokko Rytkönen, Aleksi Uusitalo, Sanna Lehenkari, Petri Sándor, George K. |
author_sort | Rytkönen, Eelis |
collection | PubMed |
description | BACKGROUND: Aggressive familial giant-cell granulomas of the jaws can be severely deforming. Surgical and nonsurgical treatments may be associated with multiple recurrences. Denosumab, a new generation antiresorptive drug, is an osteoclast inhibitor, which may be particularly useful to manage such potentially disfiguring lesions. MATERIALS AND METHODS: Two sisters, both with a history of multiple recurrent aggressive central giant-cell granuloma (CGCG)-like lesions in both jaws, were referred for management. All lesions were histologically consistent with the diagnosis of CGCG. The lesions were treated surgically with curettage and perilesional injection of triamcinolone. In particular, the older sister had four separate anatomic sites where some of her lesions had multiple recurrences necessitating three repeat procedures. A course of subcutaneous denosumab was administered following the last giant-cell granuloma removal in both sisters. RESULTS: Bony healing was normal. No further recurrences were observed over 3.5 years of follow-up after denosumab therapy in either sister. CONCLUSIONS: In this small cohort comprising two sisters with multiple aggressive recurrent giant-cell granuloma lesions at multiple sites in the mouth, subcutaneous denosumab administration was associated with success over 3.5 years of follow-up. This report cautiously adds to the clinical experience in the use of denosumab for the treatment of recurrent aggressive familial CGCG lesions. |
format | Online Article Text |
id | pubmed-6327812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63278122019-01-28 Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas Rytkönen, Eelis Ottavainen, Vuokko Rytkönen, Aleksi Uusitalo, Sanna Lehenkari, Petri Sándor, George K. Ann Maxillofac Surg Original Article - Retrospective Study BACKGROUND: Aggressive familial giant-cell granulomas of the jaws can be severely deforming. Surgical and nonsurgical treatments may be associated with multiple recurrences. Denosumab, a new generation antiresorptive drug, is an osteoclast inhibitor, which may be particularly useful to manage such potentially disfiguring lesions. MATERIALS AND METHODS: Two sisters, both with a history of multiple recurrent aggressive central giant-cell granuloma (CGCG)-like lesions in both jaws, were referred for management. All lesions were histologically consistent with the diagnosis of CGCG. The lesions were treated surgically with curettage and perilesional injection of triamcinolone. In particular, the older sister had four separate anatomic sites where some of her lesions had multiple recurrences necessitating three repeat procedures. A course of subcutaneous denosumab was administered following the last giant-cell granuloma removal in both sisters. RESULTS: Bony healing was normal. No further recurrences were observed over 3.5 years of follow-up after denosumab therapy in either sister. CONCLUSIONS: In this small cohort comprising two sisters with multiple aggressive recurrent giant-cell granuloma lesions at multiple sites in the mouth, subcutaneous denosumab administration was associated with success over 3.5 years of follow-up. This report cautiously adds to the clinical experience in the use of denosumab for the treatment of recurrent aggressive familial CGCG lesions. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6327812/ /pubmed/30693243 http://dx.doi.org/10.4103/ams.ams_192_18 Text en Copyright: © 2018 Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article - Retrospective Study Rytkönen, Eelis Ottavainen, Vuokko Rytkönen, Aleksi Uusitalo, Sanna Lehenkari, Petri Sándor, George K. Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title | Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title_full | Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title_fullStr | Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title_full_unstemmed | Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title_short | Denosumab Treatment for Aggressive Multiple Recurrent Familial Central Giant-cell Granulomas |
title_sort | denosumab treatment for aggressive multiple recurrent familial central giant-cell granulomas |
topic | Original Article - Retrospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327812/ https://www.ncbi.nlm.nih.gov/pubmed/30693243 http://dx.doi.org/10.4103/ams.ams_192_18 |
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