Risk Factors of Recurrence after Gross Total Excision in Pediatric Craniopharyngioma.

Kim, Seung Ki; Wang, Kyu Chang; Chung, Young Seob; Sim, Ki Bum; Cho, Byung Kyu

Original Article

Journal of Korean Neurosurgical Society 2001;30(1): 20-25.

Seung Ki Kim, Kyu Chang Wang, Young Seob Chung, Ki Bum Sim, Byung Kyu Cho

Division of Pediatric Neurosurgery and Clinical Research Institute, Seoul National University Hospital and Neuroscience Research Institute, SNUMRC, Seoul, Korea.

ABSTRACT

OBJECTIVE
S: A substantial number of craniopharyngiomas recur despite gross total excision. The purpose of our study was to investigate pattern of recurrence and to verify prognostic factors for recurrence after gross total excision of craniopharyngiomas in children.
METHODS
A series of 36 patients with craniopharyngiomas were reviewed. All patients had undergone gross total excision and none of them received radiotherapy after initial surgery. Fifteen were girls and twenty-one were boys, with a mean age of 7.3 years(range, one to 15 years). The mean follow-up period was 52 months(range, one to 149 months). Recurrence was noted in 14 patients within 83 months(mean 31.4 months).
RESULTS
The overall three-year recurrence free survival rate was 65%, and the five-year recurrence-free survival rate was 55%. Regular neuroimaging follow-up at six to 12-month intervals detected tumor recurrence of a smaller size 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 pitiutary fossa(n=6). Tumor location was the single significant clinical predictor of recurrence. The five-year recurrence-free survival rate was 39% for those who had an intrasellar tumor component and 81% for those who did not (p<0.05).
CONCLUSION
Craniopharyngiomas with intrasellar components should be followed cautiously and regular follow-up of patients should be emphasized, even when the tumors are totally resected.

Key Words: Pediatric craniopharyngioma; Recurrence; Gross total excision; Risk factor