Intracranial Germ Cell Tumours (GCTs) represent a rare and heterogeneous group of CNS malignancies that commonly arise in the second decade of life. They account for 0.5-11% of all intracranial neoplasms, with a male:female ratio of 2-2.5:1. Authors report a rare case of a 12-year-old female in paediatric outpatient department who presented with symptoms of raised intracranial pressure, vomiting (3-4 episodes/day), seizure and severe headache for three days associated with altered sensorium. Non