Ganglioglioma in a Survivor of Infantile Glioblastoma. J Pediatr Hematol Oncol 2020 Jan;42(1):e56-e60
Date
01/25/2019Pubmed ID
30676438DOI
10.1097/MPH.0000000000001417Scopus ID
2-s2.0-85060368706 (requires institutional sign-in at Scopus site) 2 CitationsAbstract
Congenital tumors account for 2% to 4% of all pediatric central nervous system tumors. Glioblastoma multiforme (GBM) represents a small subset of these tumors. Despite harboring histologic features similar to older patients, infants with GBM exhibit improved survival and respond more favorably to surgery and chemotherapy. To highlight this tumor's unique behavior, we report the case of a survivor of infantile GBM who developed a recurrent tumor in the surgical bed 6 months after diagnosis. The tumor was ultimately resected and was a ganglioglioma. This case shows both a favorable clinical outcome to an infantile GBM and this tumor's natural history.
Author List
Scheuermann A, Belongia M, Lawlor MW, Suchi M, Kaufman B, Vasudevaraja V, Serrano J, Snuderl M, Knipstein JAuthors
Michael W. Lawlor MD, PhD Adjunct Professor in the Pathology department at Medical College of WisconsinMariko Suchi MD, PhD Associate Professor in the Pathology department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
Brain NeoplasmsCancer Survivors
Child, Preschool
Female
Ganglioglioma
Glioblastoma
Humans
Neoplasm Recurrence, Local