OBJECTIVE: The goals of this report were to outline the clinical presentati
on, radiological characteristics, surgical techniques, postoperative morbid
ity, and long-term follow-up results for cystic jugular foramen (JF) schwan
nomas and to describe their differences, compared with solid schwannomas in
volving the JF.
METHODS: A retrospective analysis of radiological studies and surgical reco
rds identified five primarily cystic tumors among 21 cases of JF schwannoma
s that had been surgically treated at our institution.
RESULTS: Two types of cystic JF schwannomas were observed, i.e., Type 1 les
ions, which are single large cysts with thin ring-like enhancement of the t
umor wall, and Type 2 lesions, which are multiple cysts with very irregular
, thick enhancement of the cyst wall. The most common symptoms were hearing
loss, ataxia, and headaches. Total surgical removal could be performed in
all cases. The immediate postoperative findings indicated hearing improveme
nt in three cases. No deterioration of lower cranial nerve function was obs
erved. All patients were independent in the immediate postoperative period
and in the long-term follow-up period (Karnofsky Performance Scale score, 9
0).
CONCLUSION: Surgical treatment of cystic JF schwannomas can be very demandi
ng because of generally stronger adhesion of the tumor capsule to the surro
unding structures, fragile tumor capsules, and difficulty in identification
of the arachnoidal planes in some cases. Early identification of the arach
noidal planes without opening of the cyst and sharp dissection may be usefu
l. Careful intradural opening of the JF should be performed to achieve tota
l removal of the last tumor portion within the JF. A comparison of these le
sions with solid schwannomas involving the JF indicated that cystic tumors
affected a younger population, with less preoperative swallowing impairment
(P < 0.05). The immediate postoperative course in both types of cystic JF
schwannomas was usually better than for solid lesions, because of minor pos
toperative cranial nerve morbidity, especially involving lower cranial nerv
e function, in the latter cases. Long-term follow-up data failed to demonst
rate any significant differences in final patient outcomes, however.