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.