Cervicomedullary glioblastoma: A report of two cases with review of literature.

Background: Cervicomedullary glioblastoma is an extremely rare clinical entity and the principles of its management are not well understood.

Case Description: We report two cases of cervicomedullary glioblastoma in young patients aged 12 and 30 years with contrasting clinical presentation and outcomes. The 12-year-old child had rapid onset bulbar symptoms, with frank infiltration of the medulla due to which the patient succumbed within 4 weeks of surgery.