Objective
To report stripping surgery in intratemporal facial nerve schwannomas (FNS) with poor facial nerve function.
Methods
We attempted stripping surgery to completely remove intratemporal FNS with nerve intact in 17 patients, and succeeded in 12 cases. Clinical features of the tumors and the surgical approach were discussed.
Results
Multi-segment involvement was present in 10 cases (58.8%). The tumors were completely removed in all cases, and facial nerve integrity was preserved in 12 patients (70.6%). Six of 12 cases (50.0%) with nerve intact obtained acceptable facial nerve recovery, two of which recovered to Grade II, compared to 2 of 5 cases (40%) with nerve grafting.
Conclusions
Multi-segment involvement was more common in FNS. Stripping surgery could remove tumor completely with nerve intact in majority patients, and it seemed to obtain better outcomes of facial nerve.
1
Introduction
Facial nerve schwannomas (FNS) are unusual entities, and they are the most common tumors of facial nerve . FNS can involve any segments of facial nerve from cerebellar pontine angle segment to extratemporal main trunk.
There are over 600 reported intratemporal FNS in the literatures . Most reports contain relatively small case numbers, and those containing larger case series are limited. Kertesz et al. reported 88 facial nerve neuromas, but focused on anatomical and radiological features with neither clinical nor management details discussed. McMonagle et al. and O’Donoghue et al. analyzed the clinical and management details of 53 and 48 cases with FNS, respectively, but the great majority had normal or near-normal facial nerve function (House–Brackmann Grade I or Grade II). There have not been a study about a large series of intratemporal FNS with poor facial nerve function (Grade IV or worse), to our knowledge.
We aim to present a large series of intratemporal FNS with poor facial nerve function and present our experience of stripping surgery.
2
Materials and methods
A consecutive series of 17 patients of intratemporal FNS with poor facial nerve function, who were surgically treated in a tertiary referral center, were included in the study, and those patients with favorable facial nerve function (Grade III or better) who received expectant treatment other than surgical treatment were not involved. All diagnoses were confirmed pathologically. The stripping procedure was accomplished by the same surgeon. Intraoperatvie facial nerve monitoring and electrical stimulation were introduced to aid identification of facial nerve from the tumor tissues, and the key procedure was meticulous microdissection between nerve fibers and the tumor tissue under high magnification. The separation of fascicle and the tumors must be gentle to avoid facial nerve damage. Facial nerve was sacrificed when it was impossible to separate facial nerve from the tumors, and sural or greater auricular nerve was used as graft to fill the nerve deficit. Whether greater auricular nerve or sural nerve was used as the graft material was dependent on the length of nerve graft required. Greater auricular nerve was the preferred choice, since it was convenient to harvest, but sural nerve was adopted when longer nerve graft was required.
The surgical approach was mainly determined by tumor location. If the tumors were located at labyrinthine segment, geniculate ganglion, tympanic segment, or mastoid segment, transmastoid approach would be used. Middle cranial fossa combined with transmastoid approach was adopted when internal auditory canal was also affected. For adequate exposure of the region at geniculate ganglion or labyrinthine segment, incus was removed and placed back after tumor removal. The incus should be repositioned exactly to minimize hearing damage.
There were 9 female and 8 male among the case series, and mean age was 35.65 ± 1.53 years (range, 17 to 66 years). They were followed up for 43.94 ± 2.14 months (range, 15 to 80 months), with MRI examination to assess tumor recurrence. Hearing was measured by clinical audiometer. Their clinical features and outcomes of facial nerve are discussed.
2
Materials and methods
A consecutive series of 17 patients of intratemporal FNS with poor facial nerve function, who were surgically treated in a tertiary referral center, were included in the study, and those patients with favorable facial nerve function (Grade III or better) who received expectant treatment other than surgical treatment were not involved. All diagnoses were confirmed pathologically. The stripping procedure was accomplished by the same surgeon. Intraoperatvie facial nerve monitoring and electrical stimulation were introduced to aid identification of facial nerve from the tumor tissues, and the key procedure was meticulous microdissection between nerve fibers and the tumor tissue under high magnification. The separation of fascicle and the tumors must be gentle to avoid facial nerve damage. Facial nerve was sacrificed when it was impossible to separate facial nerve from the tumors, and sural or greater auricular nerve was used as graft to fill the nerve deficit. Whether greater auricular nerve or sural nerve was used as the graft material was dependent on the length of nerve graft required. Greater auricular nerve was the preferred choice, since it was convenient to harvest, but sural nerve was adopted when longer nerve graft was required.
The surgical approach was mainly determined by tumor location. If the tumors were located at labyrinthine segment, geniculate ganglion, tympanic segment, or mastoid segment, transmastoid approach would be used. Middle cranial fossa combined with transmastoid approach was adopted when internal auditory canal was also affected. For adequate exposure of the region at geniculate ganglion or labyrinthine segment, incus was removed and placed back after tumor removal. The incus should be repositioned exactly to minimize hearing damage.
There were 9 female and 8 male among the case series, and mean age was 35.65 ± 1.53 years (range, 17 to 66 years). They were followed up for 43.94 ± 2.14 months (range, 15 to 80 months), with MRI examination to assess tumor recurrence. Hearing was measured by clinical audiometer. Their clinical features and outcomes of facial nerve are discussed.
3
Results
Summary of the cases is listed in Table 1 .
Case no. | Location | Symptoms | FP duration (years) | Onset | PreFNF | PostFNF | SA | Nerve graft | FU (months) | Initial HL (dB) | Final HL (dB) |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | GG | FP | 8 | Recurrent | VI | VI | TM | No | 58 | 10 | 10 |
2 | TS, MT | FP, CHL, T | 7 | Insidious | VI | IV | TM | SN | 80 | 40 | 20 |
3 | TS | FP, CHL, T | 1 | Sudden | VI | IV | TM | GAN | 76 | 50 | 35 |
4 | IAC till MS | FP, V, MHL, otalgia | 2/12 | Sudden | VI | IV | MCF, TM | No | 60 | 55 | 55 |
5 | IAC till MS | FP, V, SNHL | 2/12 | Sudden | V | III | MCF, TM | GAN | 42 | 45 | 45 |
6 | GG | FP, xerophthalmia | 18 | Insidious | V | III | TM | No | 24 | 10 | 10 |
7 | IAC, TS | FP, CHL | 7 | Insidious | VI | VI | MCF, TM | No | 62 | 45 | 15 |
8 | GG, TS, MS, MT | FP | 2 | Insidious | VI | III | TM | No | 50 | 5 | 20 |
9 | GG, LS | FP, otalgia | 3/12 | Sudden | V | II | TM | No | 29 | 15 | 20 |
10 | LS | FP, otalgia | 17 | Insidious | VI | IV | TM | No | 20 | 10 | 20 |
11 | MS | FP, otalgia | 3/12 | Sudden | VI | III | TM | No | 25 | 15 | 15 |
12 | TS | FP, CHL, T | 10 | Insidious | VI | VI | TM | No | 61 | 35 | 15 |
13 | LS, GG, TS | FP, dysgeusia | 2 | Insidious | V | V | TM | GAN | 15 | 10 | 25 |
14 | LS, GG, MS, MT FP, CHL, V | 50 | Sudden | VI | VI | TM | No | 18 | 60 | 45 | |
15 | TS, MS | FP | 1 | Insidious | IV | III | TM | SN | 30 | 10 | 10 |
16 | LS | FP | 3/12 | Sudden | IV | II | TM | No | 66 | 15 | 15 |
17 | LS, TS | FP | 1 | Insidious | V | III | TM | No | 31 | 10 | 20 |