Childs Nerv Syst. 2025 Jul 30;41(1):249. doi: 10.1007/s00381-025-06908-z.
ABSTRACT
INTRODUCTION: Brainstem tumors represent 15% of brain tumors in children. Eighty percent of these tumors are diffuse pontine tumors with a globally poor prognosis even with the tailored chemotherapies and radiotherapy. Twenty percent of these tumors are benign and present a good prognosis with only a surgical treatment.
MATERIAL: All patients admitted with the diagnosis of brainstem tumor in the Pediatric Neurosurgical Department between January 1997 and December 2021 have been considered for this study. We excluded patients with a diagnosis of DIPG or any other malignant histopathology.
RESULTS: Out of 112 patients with a brainstem tumor, 42 patients had a proved benign histological diagnosis and were included in this study. The average age, at diagnosis, was 8 years old, with a median age of 4.7 years. All patients were operated. Forty-eight surgical procedures were realized for the 42 patients: 8 biopsies and 40 direct approaches. Seventeen patients had a surgical treatment for hydrocephalus. Regarding surgical outcome, eight patients presented motor deficits, six improved, while in other two, the deficit was unchanged but not impeding the walk. The major clinical complication after surgery was cranial nerve palsy, present in 18 patients. Two patients deceased in the early postoperative period and two patients for a recurrence after 7 and 8 years after the diagnosis. Thirty-eight patients are alive.
CONCLUSION: Benign brainstem tumors can be associated with a favorable evolution, a low growing rate, and, when symptomatic, curable with surgery. The surgical resection has to be safe and reasonable to avoid catastrophic complications. The results of surgery are particularly conditioned by the skills and experience of the surgeon.
PMID:40731067 | DOI:10.1007/s00381-025-06908-z
