Radical excision of pediatric craniopharyngioma: recurrence pattern and prognostic factors

Citation
Sk. Kim et al., Radical excision of pediatric craniopharyngioma: recurrence pattern and prognostic factors, CHILD NERV, 17(9), 2001, pp. 531-536
Citations number
25
Categorie Soggetti
Pediatrics
Journal title
CHILDS NERVOUS SYSTEM
ISSN journal
02567040 → ACNP
Volume
17
Issue
9
Year of publication
2001
Pages
531 - 536
Database
ISI
SICI code
0256-7040(200109)17:9<531:REOPCR>2.0.ZU;2-9
Abstract
The purpose of our study was to investigate the pattern of recurrence and t he prognostic factors for recurrence of pediatric craniopharyngiomas after radical excision. A series of 36 patients with craniopharyngiomas (21 boys and 15 girls; age range 1-15 years; mean 7.3 years) were reviewed. All pati ents had undergone radical excision without radiotherapy. The mean follow-u p period was 52 months (range 1-149 months). Tumors recurred in 14 patients within 83 months (mean 31.4 months). The overall 5-year recurrence-free su rvival rate was 55%. Regular neuroimaging follow-up detected tumor recurren ce while the lesions were still small before symptoms developed (P <0.05). At the first surgical procedure, the optic nerve/chiasm (n=23) was the most common adhesion site. The most frequent sites of recurrence were the optic nerve/chiasm (n=6) and the pituitary fossa (n=6). Tumor location was the s ingle significant clinical predictor of recurrence. The 5-year recurrence-f ree survival rate was 39% for those who had an intrasellar tumor component and 81% for those who did not (P <0.05). The Ki-67 labeling indices (LIs) o f primary tumors did not have prognostic value for recurrence. Recurrent tu mors tended to have higher Ki-67 Us than their primary counterparts. On the basis of this study, we concluded that craniopharyngiomas with intrasellar components should be followed cautiously and the necessity for regular fol low-up should be emphasized, even when the tumor is "totally" resected.