Parinaud Syndrome and Obstructive Hydrocephalus as Initial Manifestations of an AFP-Secreting Pineal Region Germ Cell Tumor: A Case Report
DOI:
https://doi.org/10.3126/njr.v15i2.95812Keywords:
alpha-Fetoproteins, Ocular Motility Disorders, VentriculostomyAbstract
A 14-year-old male presented with Parinaud syndrome, obstructive hydrocephalus, and markedly elevated serum AFP (272 ng/mL) and β-hCG (317 mIU/mL), suggesting a non-germinomatous germ cell tumor (NGGCT) of the pineal region. MRI confirmed a pineal mass with pituitary stalk involvement. Endoscopic third ventriculostomy (ETV) relieved hydrocephalus and enabled CSF tumor marker sampling. Four cycles of CE/IE chemotherapy achieved complete biochemical remission with significant neurological recovery. This case highlights the neuro-ophthalmic clues to early pineal GCT diagnosis and the effectiveness of ETV combined with chemotherapy.
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