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Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses
BACKGROUND: Ameloblastic carcinoma and metastasising ameloblastoma are rare epithelial odontogenic tumours with aggressive features. Distinguishing between these two lesions is often clinically difficult but necessary to predict tumour behaviour or to plan future therapy. Here, we provide a brief re...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423427/ https://www.ncbi.nlm.nih.gov/pubmed/37573343 http://dx.doi.org/10.1186/s12903-023-03259-6 |
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author | Hurník, Pavel Putnová, Barbora Moldovan Ševčíková, Tereza Hrubá, Eva Putnová, Iveta Škarda, Josef Havel, Martin Res, Oldřich Cvek, Jakub Buchtová, Marcela Štembírek, Jan |
author_facet | Hurník, Pavel Putnová, Barbora Moldovan Ševčíková, Tereza Hrubá, Eva Putnová, Iveta Škarda, Josef Havel, Martin Res, Oldřich Cvek, Jakub Buchtová, Marcela Štembírek, Jan |
author_sort | Hurník, Pavel |
collection | PubMed |
description | BACKGROUND: Ameloblastic carcinoma and metastasising ameloblastoma are rare epithelial odontogenic tumours with aggressive features. Distinguishing between these two lesions is often clinically difficult but necessary to predict tumour behaviour or to plan future therapy. Here, we provide a brief review of the literature available on these two types of lesions and present a new case report of a young man with an ameloblastoma displaying metastatic features. We also use this case to illustrate the similarities and differences between these two types of tumours and the difficulties of their differential diagnosis. CASE PRESENTATION: Our histopathological analyses uncovered a metastasising tumour with features of ameloblastic carcinoma, which developed from the ameloblastoma. We profiled the gene expression of Wnt pathway members in ameloblastoma sample of this patient, because multiple molecules of this pathway are involved in the establishing of cell polarity, cell migration or for epithelial–mesenchymal transition during tumour metastasis to evaluate features of tumor behaviour. Indeed, we found upregulation of several cell migration–related genes in our patient. Moreover, we uncovered somatic mutation BRAF p.V600E with known pathological role in cancerogenesis and germline heterozygous FANCA p.S858R mutation, whose interpretation in this context has not been discussed yet. CONCLUSIONS: In conclusion, we have uncovered a unique case of ameloblastic carcinoma associated with an alteration of Wnt signalling and the presence of BRAF mutation. Development of harmful state of our patient might be also supported by the germline mutation in one FANCA allele, however this has to be confirmed by further analyses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-023-03259-6. |
format | Online Article Text |
id | pubmed-10423427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104234272023-08-14 Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses Hurník, Pavel Putnová, Barbora Moldovan Ševčíková, Tereza Hrubá, Eva Putnová, Iveta Škarda, Josef Havel, Martin Res, Oldřich Cvek, Jakub Buchtová, Marcela Štembírek, Jan BMC Oral Health Case Report BACKGROUND: Ameloblastic carcinoma and metastasising ameloblastoma are rare epithelial odontogenic tumours with aggressive features. Distinguishing between these two lesions is often clinically difficult but necessary to predict tumour behaviour or to plan future therapy. Here, we provide a brief review of the literature available on these two types of lesions and present a new case report of a young man with an ameloblastoma displaying metastatic features. We also use this case to illustrate the similarities and differences between these two types of tumours and the difficulties of their differential diagnosis. CASE PRESENTATION: Our histopathological analyses uncovered a metastasising tumour with features of ameloblastic carcinoma, which developed from the ameloblastoma. We profiled the gene expression of Wnt pathway members in ameloblastoma sample of this patient, because multiple molecules of this pathway are involved in the establishing of cell polarity, cell migration or for epithelial–mesenchymal transition during tumour metastasis to evaluate features of tumor behaviour. Indeed, we found upregulation of several cell migration–related genes in our patient. Moreover, we uncovered somatic mutation BRAF p.V600E with known pathological role in cancerogenesis and germline heterozygous FANCA p.S858R mutation, whose interpretation in this context has not been discussed yet. CONCLUSIONS: In conclusion, we have uncovered a unique case of ameloblastic carcinoma associated with an alteration of Wnt signalling and the presence of BRAF mutation. Development of harmful state of our patient might be also supported by the germline mutation in one FANCA allele, however this has to be confirmed by further analyses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-023-03259-6. BioMed Central 2023-08-12 /pmc/articles/PMC10423427/ /pubmed/37573343 http://dx.doi.org/10.1186/s12903-023-03259-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . 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 in a credit line to the data. |
spellingShingle | Case Report Hurník, Pavel Putnová, Barbora Moldovan Ševčíková, Tereza Hrubá, Eva Putnová, Iveta Škarda, Josef Havel, Martin Res, Oldřich Cvek, Jakub Buchtová, Marcela Štembírek, Jan Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title | Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title_full | Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title_fullStr | Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title_full_unstemmed | Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title_short | Metastasising ameloblastoma or ameloblastic carcinoma? A case report with mutation analyses |
title_sort | metastasising ameloblastoma or ameloblastic carcinoma? a case report with mutation analyses |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423427/ https://www.ncbi.nlm.nih.gov/pubmed/37573343 http://dx.doi.org/10.1186/s12903-023-03259-6 |
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