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Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma

Yolk sac tumor (YST) and teratoma both categorized as germ cell tumor (GCT). YST shows preferential differentiation toward yolk sac structures, while teratoma consists of tissues that originate from at least two embryonic germinal layers. Extragonadal location of YST is rare, whereas extragonadal te...

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Autores principales: Rahadiani, Nur, Krisnuhoni, Ening, Stephanie, Marini, Handjari, Diah Rini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421921/
https://www.ncbi.nlm.nih.gov/pubmed/30967724
http://dx.doi.org/10.4103/jomfp.JOMFP_127_18
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author Rahadiani, Nur
Krisnuhoni, Ening
Stephanie, Marini
Handjari, Diah Rini
author_facet Rahadiani, Nur
Krisnuhoni, Ening
Stephanie, Marini
Handjari, Diah Rini
author_sort Rahadiani, Nur
collection PubMed
description Yolk sac tumor (YST) and teratoma both categorized as germ cell tumor (GCT). YST shows preferential differentiation toward yolk sac structures, while teratoma consists of tissues that originate from at least two embryonic germinal layers. Extragonadal location of YST is rare, whereas extragonadal teratoma is majority presented in nasopharynx area. Mature teratoma tends to be benign although some malignant transformation can occur. Recurrence of teratoma was reported mostly in the case of immature teratoma. YST occurrence after removal of mature teratoma is never reported. It is extremely rare for a second GCT to occur at the same site and with a different histological type. We herein report a case of a female infant presented with YST following a congenital buccal mature teratoma.
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spelling pubmed-64219212019-04-09 Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma Rahadiani, Nur Krisnuhoni, Ening Stephanie, Marini Handjari, Diah Rini J Oral Maxillofac Pathol Case Report Yolk sac tumor (YST) and teratoma both categorized as germ cell tumor (GCT). YST shows preferential differentiation toward yolk sac structures, while teratoma consists of tissues that originate from at least two embryonic germinal layers. Extragonadal location of YST is rare, whereas extragonadal teratoma is majority presented in nasopharynx area. Mature teratoma tends to be benign although some malignant transformation can occur. Recurrence of teratoma was reported mostly in the case of immature teratoma. YST occurrence after removal of mature teratoma is never reported. It is extremely rare for a second GCT to occur at the same site and with a different histological type. We herein report a case of a female infant presented with YST following a congenital buccal mature teratoma. Medknow Publications & Media Pvt Ltd 2019-02 /pmc/articles/PMC6421921/ /pubmed/30967724 http://dx.doi.org/10.4103/jomfp.JOMFP_127_18 Text en Copyright: © 2019 Journal of Oral and Maxillofacial Pathology 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 Case Report
Rahadiani, Nur
Krisnuhoni, Ening
Stephanie, Marini
Handjari, Diah Rini
Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title_full Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title_fullStr Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title_full_unstemmed Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title_short Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
title_sort extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421921/
https://www.ncbi.nlm.nih.gov/pubmed/30967724
http://dx.doi.org/10.4103/jomfp.JOMFP_127_18
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