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Multiple malignant transformations of an ovarian mature cystic teratoma

BACKGROUND: Malignant transformation of mature cystic teratomas (MCTs) is a rare phenomenon. The most common histology of a malignant transformation is squamous cell carcinoma, and there are limited reports of multiple malignancies arising in a single MCT. Further data are necessary to guide managem...

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Autores principales: Cagino, Kristen, Levitan, Daniel, Schatz-Siemers, Nina, Zarnegar, Rasa, Chapman-Davis, Eloise, Holcomb, Kevin, Frey, Melissa K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105337/
https://www.ncbi.nlm.nih.gov/pubmed/32256692
http://dx.doi.org/10.3332/ecancer.2020.1009
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author Cagino, Kristen
Levitan, Daniel
Schatz-Siemers, Nina
Zarnegar, Rasa
Chapman-Davis, Eloise
Holcomb, Kevin
Frey, Melissa K
author_facet Cagino, Kristen
Levitan, Daniel
Schatz-Siemers, Nina
Zarnegar, Rasa
Chapman-Davis, Eloise
Holcomb, Kevin
Frey, Melissa K
author_sort Cagino, Kristen
collection PubMed
description BACKGROUND: Malignant transformation of mature cystic teratomas (MCTs) is a rare phenomenon. The most common histology of a malignant transformation is squamous cell carcinoma, and there are limited reports of multiple malignancies arising in a single MCT. Further data are necessary to guide management of these atypical cases. CASE: We present the case of a 48-year-old with MCT containing a malignant papillary thyroid carcinoma (PTC) arising in the context of struma ovarii and a carcinoid tumour. CONCLUSION: Malignant transformations of MCTs are exceedingly rare with no guidelines on management. We use this case to demonstrate an approach for the workup and management of malignantly transformed MCTs.
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spelling pubmed-71053372020-04-01 Multiple malignant transformations of an ovarian mature cystic teratoma Cagino, Kristen Levitan, Daniel Schatz-Siemers, Nina Zarnegar, Rasa Chapman-Davis, Eloise Holcomb, Kevin Frey, Melissa K Ecancermedicalscience Case Report BACKGROUND: Malignant transformation of mature cystic teratomas (MCTs) is a rare phenomenon. The most common histology of a malignant transformation is squamous cell carcinoma, and there are limited reports of multiple malignancies arising in a single MCT. Further data are necessary to guide management of these atypical cases. CASE: We present the case of a 48-year-old with MCT containing a malignant papillary thyroid carcinoma (PTC) arising in the context of struma ovarii and a carcinoid tumour. CONCLUSION: Malignant transformations of MCTs are exceedingly rare with no guidelines on management. We use this case to demonstrate an approach for the workup and management of malignantly transformed MCTs. Cancer Intelligence 2020-02-04 /pmc/articles/PMC7105337/ /pubmed/32256692 http://dx.doi.org/10.3332/ecancer.2020.1009 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Cagino, Kristen
Levitan, Daniel
Schatz-Siemers, Nina
Zarnegar, Rasa
Chapman-Davis, Eloise
Holcomb, Kevin
Frey, Melissa K
Multiple malignant transformations of an ovarian mature cystic teratoma
title Multiple malignant transformations of an ovarian mature cystic teratoma
title_full Multiple malignant transformations of an ovarian mature cystic teratoma
title_fullStr Multiple malignant transformations of an ovarian mature cystic teratoma
title_full_unstemmed Multiple malignant transformations of an ovarian mature cystic teratoma
title_short Multiple malignant transformations of an ovarian mature cystic teratoma
title_sort multiple malignant transformations of an ovarian mature cystic teratoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105337/
https://www.ncbi.nlm.nih.gov/pubmed/32256692
http://dx.doi.org/10.3332/ecancer.2020.1009
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