| Literature DB >> 31620699 |
Jeyasakthy Saniasiaya1, Suzina Sheikh Ab Hamid1, Hazama Mohamad1, Wan Nur Najmiyah Wan Abdul Wahab1, Norzaliana Zawawi1.
Abstract
Paediatric germ cell tumor is composed of various neoplasms which exhibit capricious clinical presentation and histological features depending on the age and the area of presentation. Yolk sac tumor is an extremely rare malignant tumor of embryonic origin which usually arises from the gonads. Its manifestation in the head and neck region is extremely rare. Here, we report a rare case of the malignant transformation of mature teratoma into yolk sac tumor of the neck in an infant. Diagnosis was confirmed following histopathological examination of the neck mass along with marked increase of the serum alpha-fetoprotein. The child unfortunately succumbed prior to chemotherapy. We highlight the challenge we faced in diagnosing and managing this rare entity. We would also like to recommend serial monitoring of serum alpha-fetoprotein in all patients with mature teratoma to detect malignant transformation early. © Copyright 2019 by Official Journal of the Turkish Society of Otorhinolaryngology and Head and Neck Surgery.Entities:
Keywords: Germ cell tumor; malignant transformation; teratoma; yolk sac tumor
Year: 2019 PMID: 31620699 PMCID: PMC6779102 DOI: 10.5152/tao.2019.3900
Source DB: PubMed Journal: Turk Arch Otorhinolaryngol ISSN: 2667-7466