One suprasellar, one mesencephalic, and nine cerebellar hemangioblasto
mas were treated with the gamma knife in 10 patients (median age 48 ye
ars) in Stockholm between 1978 and 1993. Four patients had von Hippel-
Lindau dis ease, a dominant inherited trait predisposing to multiple h
emangioblastomas. Six hemangioblastomas were treated with radiotherapy
at a median margin dose of 25 Gy (20-35 Gy) before 1990 and the next
five with a median of 10 Gy (5-19 Gy). Computerized tomography or magn
etic resonance images were available for 10 of the 11 hemangioblastoma
s at a median follow-up time of 26 months (4-68 months) after radiosur
gery. The solid part of six hemangioblastomas shrank in a median of 30
months, whereas four hemangioblastomas were unchanged at a median of
14 months. Five hemangioblastomas had an adjoining cyst and three of t
hese cysts had to be evacuated after radiosurgery. One solitary hemang
ioblastoma later developed a de novo cyst that also needed evacuation.
One patient with two cerebellar hemangioblastomas (margin dose 25 Gy
each) developed edema at 6 months and required a shunt and prolonged c
orticosteroid treatment. The combined follow-up data of the 23 hemangi
oblastomas in 15 patients from previous literature and the present ser
ies indicate that, first, a solitary small- or medium-sized hemangiobl
astoma usually shrinks or stops growing after radiosurgery. The recomm
ended margin dose is 10 to 15 Gy. Second, the adjoining cyst often doe
s not respond to radiosurgery but requires later, sometimes repeated e
vacuation.