DOI: 10.36347/sjmcr.2022.v10i08.009

Pages: 783-785

Spinal Hemangioblastomas are rare benign vascular tumors of the central nervous system presenting in adults and are seen in association with VHL gene mutation. MRI is the preliminary diagnostic modality whereas histopathological diagnosis after complete surgical resection of tumor remains a confirmatory modality. Here we present an extremely rare case of a 2 year old female child with complaints of lower limb weakness who was diagnosed histopathologically with spinal hemangioblastoma.