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Congenital mixed malignant germ cell tumor involving cerebrum and orbit

  • Jui Chi Lee*
  • , Shih Ming Jung
  • , An Shine Chao
  • , Chuen Hsueh
  • *Corresponding author for this work
  • China Medical University Taichung
  • Chang Gung Memorial Hospital

Research output: Contribution to journal › Journal Article › peer-review

19 Scopus citations

Abstract

Congenital intracranial tumors are rare and only account for 0.5 to 1.5 % of all pediatric brain tumors. Teratoma is the most frequently encountered intracranial tumor at birth. Cephalomegaly and hydrocephalus are the usual clinical presentations. Advances in imaging techniques have improved diagnostic accuracy in congenital brain tumors. But the prognosis of a massive intracranial teratoma is always dismal. We report a congenital mixed malignant germ cell tumor in a male fetus at 27 weeks of gestation, with massive involvement of cerebrum and orbit. According to histological and immunohistochemical studies, the tumor was made up of predominantly immature teratoma combined with a yolk sac tumor. To our knowledge, such a combination has not been well documented in the literature.

Original languageEnglish
Pages (from-to)261-265
Number of pages5
JournalJournal of Perinatal Medicine
Volume31
Issue number3
DOIs
StatePublished - 2003
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Congenital
  • Intracranial
  • Mixed malignant germ cell tumor
  • Orbital
  • Teratoma
  • Yolk sac tumor

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