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An interesting case-report of ex-ameloblastic carcinoma
Ameloblastoma (AM) is considered one of the most common lesions of odontogenic origin. Although it is always considered as benign neoplasm, ameloblastic carcinoma (AC) represents its malignant counterpart. It is characterized by the expansion of jaws, rapid growth, and a perforated cortex with well-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581286/ https://www.ncbi.nlm.nih.gov/pubmed/37854922 http://dx.doi.org/10.4103/jomfp.jomfp_7_23 |
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author | Tomar, Sanjeev Tomar, Upma Singh, Richa Verma, Nancy |
author_facet | Tomar, Sanjeev Tomar, Upma Singh, Richa Verma, Nancy |
author_sort | Tomar, Sanjeev |
collection | PubMed |
description | Ameloblastoma (AM) is considered one of the most common lesions of odontogenic origin. Although it is always considered as benign neoplasm, ameloblastic carcinoma (AC) represents its malignant counterpart. It is characterized by the expansion of jaws, rapid growth, and a perforated cortex with well-defined unilocular/multilocular radiolucent lesions. To confirm the diagnosis of AM and AC is extremely crucial. Immunohistochemistry such as SOX2 and Ki67 plays a significant role in the confirmation of diagnosis. Management of these cases is from surgical excision with radical neck dissection. The prognosis is poor with only 5 years of survival. This review presents an interesting case of ex-AC, in which the patient was diagnosed at the same site with peripheral AM 1 year ago. |
format | Online Article Text |
id | pubmed-10581286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-105812862023-10-18 An interesting case-report of ex-ameloblastic carcinoma Tomar, Sanjeev Tomar, Upma Singh, Richa Verma, Nancy J Oral Maxillofac Pathol Case Report Ameloblastoma (AM) is considered one of the most common lesions of odontogenic origin. Although it is always considered as benign neoplasm, ameloblastic carcinoma (AC) represents its malignant counterpart. It is characterized by the expansion of jaws, rapid growth, and a perforated cortex with well-defined unilocular/multilocular radiolucent lesions. To confirm the diagnosis of AM and AC is extremely crucial. Immunohistochemistry such as SOX2 and Ki67 plays a significant role in the confirmation of diagnosis. Management of these cases is from surgical excision with radical neck dissection. The prognosis is poor with only 5 years of survival. This review presents an interesting case of ex-AC, in which the patient was diagnosed at the same site with peripheral AM 1 year ago. Wolters Kluwer - Medknow 2023 2023-07-13 /pmc/articles/PMC10581286/ /pubmed/37854922 http://dx.doi.org/10.4103/jomfp.jomfp_7_23 Text en Copyright: © 2023 Journal of Oral and Maxillofacial Pathology https://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 | Case Report Tomar, Sanjeev Tomar, Upma Singh, Richa Verma, Nancy An interesting case-report of ex-ameloblastic carcinoma |
title | An interesting case-report of ex-ameloblastic carcinoma |
title_full | An interesting case-report of ex-ameloblastic carcinoma |
title_fullStr | An interesting case-report of ex-ameloblastic carcinoma |
title_full_unstemmed | An interesting case-report of ex-ameloblastic carcinoma |
title_short | An interesting case-report of ex-ameloblastic carcinoma |
title_sort | interesting case-report of ex-ameloblastic carcinoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581286/ https://www.ncbi.nlm.nih.gov/pubmed/37854922 http://dx.doi.org/10.4103/jomfp.jomfp_7_23 |
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