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Updated: Jun 16, 2026

Endoscopic Third Ventriculostomy and Pineal Biopsy from a Single Entry Point
Published on: June 28, 2024
Case Report: Primary choriocarcinoma of the pineal region
Mengxing Wu1,2, Wei Xia3
1Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Wuhan Maternal and Child Healthcare Hospital, Wuhan University of Science and Technology, Postgraduate Training Base, Wuhan, China.
Abstract:
Primary intracranial choriocarcinoma (PICCC) is a rare, highly malignant non-germinomatous germ cell tumor (NGGCT), primarily affecting children and adolescents with a male predominance. It most commonly arises in the pineal region and sella turcica. This report describes a case of primary choriocarcinoma in the pineal region. CT imaging revealed a patchy area of abnormal high density with slight internal density variation and small nodular calcifications. MRI showed a mixed signal pattern, predominantly slightly short T1-weighted and short T2-weighted signals. Contrast-enhanced imaging demonstrated heterogeneous enhancement. Surgical pathology specimens showed immunohistochemical positivity for HCG(+), HPL(+), CK(PAN)(+), EMA(partial+), p53(partial+), PLAP(placental alkaline phosphatase, partial+), CD117(partial+), and Ki-67 proliferation index: 20%. The pathological findings were consistent with pineal region choriocarcinoma. The patient's serum β-HCG level decreased to <0.1 mIU/mL one year after surgery, and the child remained in good condition without recurrence during the 2-year follow-up.
