Residual or Recurrent Cerebellar Low-Grade Glioma in Children after Tumor Resection: Is Re-Treatment Needed? A Single Center Experience from 1983 to 2003
Authors:
- Martin BeneschMBMartin Benesch
- Hans-Georg EderHEHans-Georg Eder
- Petra SovinzPSPetra Sovinz
- Johann RaithJRJohann Raith
- Herwig LacknerHLHerwig Lackner
- Andrea MoserAMAndrea Moser
- Christian UrbanCUChristian Urban
- 1 April 2006
- journal article
- research article
- Published by S. Karger AG in Pediatric Neurosurgery
- Vol. 42 (3) , 159-164
Abstract
Purpose:The aim of this study was to report on children with cerebellar low-grade glioma (LGG), who were found to have progressive or nonprogresssive residual tumors or tumor recurrence after tumor resection. Patients and Methods: Medical records and magnetic resonance imaging (MRI) studies of children (Results: Of 289 patients with CNS tumors referred between 1983 and 2003, 28 (9.7%) (15 male, 13 female; median age at diagnosis: 71 months) had cerebellar LGG (pilocytic astrocytoma grade I: n = 21; fibrillary astrocytoma grade II: n = 5; mixed hamartoma/pilocytic astrocytoma: n = 1; radiographic diagnosis: n = 1). Total resection was initially performed in 16 patients (57.1%), near total resection in 4 (14.3%), and partial resection in 6 patients (21.4%). One patient underwent biopsy. At a median follow-up of 112 months, 25 patients (89.3%) were alive, 18 of them being in complete remission. Three patients died, 2 due to symptoms related to brain stem compression/infiltration and 1 patient due to postoperative cerebral edema. Presently 5 patients have nonprogressive residual tumors and 2 patients developed nonprogressive recurrences 10 years and 20 months after initial total resection, respectively. None of them required second surgery and none received additional nonsurgical therapies. Only 1 additional patient had to undergo second surgery due to disease progression. Conclusions: A ‘wait and see’ strategy is justified in patients with nonprogressive recurrent or residual cerebellar LGG after primary tumor resection. However, long-term follow-up with repeated MRI is mandatory in these patients to detect disease progression. Second surgery is indicated only in patients with unequivocal disease progression, as documented by MRI.Keywords
This publication has 20 references indexed in Scilit:
- Sub-classification of low-grade cerebellar astrocytoma: is it clinically meaningful?Child's Nervous System, 2003
- Pilocytic Astrocytomas in Children: Prognostic Factors—A Retrospective Study of 80 CasesNeurosurgery, 2003
- Benign cerebellar astrocytomas in childrenJournal of Neurosurgery, 1999
- Cerebellar astrocytomas in childrenJournal of Neuro-Oncology, 1996
- Brain Tumors in ChildrenNew England Journal of Medicine, 1994
- Astrocytomas of the cerebellum: A comparative clinicopathologic study of pilocytic and diffuse astrocytomasCancer, 1993
- Histological Typing of Tumours of the Central Nervous System1993
- Benign Cerebellar Astrocytomas of ChildhoodNeurosurgery, 1992
- Importance of histologic condition and treatment of pediatric cerebellar astrocytomaCancer, 1991
- Childhood cerebellar astrocytomas: Is there a role for postoperative irradiation?International Journal of Radiation Oncology - Biology - Physics (IJROBP), 1990