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Extragonadal yolk sac tumor following congenital buccal mature cystic teratoma
Author(s) -
Nur Rahadiani,
Ening Krisnuhoni,
Marini Stephanie,
Diah Rini Handjari
Publication year - 2019
Publication title -
journal of oral and maxillofacial pathology/journal of oral and maxillofacial pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.455
H-Index - 25
eISSN - 1998-393X
pISSN - 0973-029X
DOI - 10.4103/jomfp.jomfp_127_18
Subject(s) - yolk sac , teratoma , immature teratoma , pathology , biology , germ cell tumors , mature teratoma , anatomy , malignant transformation , germ cell , embryo , medicine , chemotherapy , biochemistry , genetics , gene , microbiology and biotechnology
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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