Posterior fossa astroblastoma in a child: a case report and a review of the literature.
Özlem YapıcıerMustafa Kemal DemirUmut ÖzdamarlarDeniz KılıçAkın AkakınTürker KılıçPublished in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2019)
A 4-year-old girl presented to the hospital with a progressive headache, difficulty walking, and persistent daily vomiting for 3 weeks. Papilledema was observed on fundoscopic examination. A large left cerebellovermian tumor with "bubbly" appearance was discovered. Total removal of the tumor mass was performed, and a diagnosis of low-grade astroblastoma was made. Adjuvant radiotherapy was performed due to the risk of recurrence. The patient is disease-free and has been kept on close follow-up for 6 months. The occurrence of posterior fossa astroblastoma has been rarely reported in the literature. Thus, when a "bubby" appearance enhancing cystic solid tumor is located on the cerebellar hemisphere in a child, an astroblastoma should also be included in the differential diagnosis.