Revision Surgery for Vestibular Schwannomas

Abstract

Objectives To describe clinical outcomes of patients undergoing revision surgery for vestibular schwannomas.

Design Retrospective case series.

Setting Tertiary private neurotologic practice.

Participants Patients who underwent revision surgeries for recurrent/residual vestibular schwannomas between 1985 and 2015.

Main Outcome Measures Degree of resection, facial nerve function, cerebrospinal fluid (CSF) leak.

Results A total of 234 patients underwent 250 revision surgeries for recurrent/residual vestibular schwannomas. Of these, 86 carried a diagnosis of neurofibromatosis type 2 (NF2). The mean number of prior surgeries was 1.26, and 197 (85%) prior surgeries had been performed elsewhere. The average age at surgery was 43. The most common approach employed at the time of revision surgery was translabyrinthine (87%), followed by transcochlear (6%), middle fossa (5%), and retrosigmoid (2%). Gross total resection was achieved in 212 revision surgeries (85%). Preoperative House–Brackmann facial nerve function was similar in non-NF2 and NF2 groups (mean: 2.7). Mean postoperative facial nerve function at last follow-up was 3.8 in the non-NF2 group and 3.9 in the NF2 group. History of radiation and the extent of resection were not associated with differences in facial nerve function preoperatively or postoperatively. CSF leaks occurred after 21 surgeries (8%), and six (2%) patients required reoperation.

Conclusions This is the largest series of revision surgery for vestibular schwannomas to date. Our preferred approach is the translabyrinthine craniotomy, which can be readily modified to include the transcochlear approach for improved access. CSF leak rate slightly exceeds that of primary surgery, and gross total resection is achievable in the vast majority of patients.

Keywords

vestibular schwannoma - acoustic neuroma - translabyrinthine approach - retrosigmoid approach - middle fossa approach - microsurgery

Introduction

Vestibular schwannomas are benign neoplasms of the vestibular nerve occurring in the internal auditory canal (IAC) and cerebellopontine angle. Their incidence has been estimated at 2 per 100,000 individuals.[1] Options for the management of vestibular schwannomas include observation, stereotactic radiation, and microsurgical resection. While the average growth rate for vestibular schwannomas is approximately 1.2 mm per year,[2] individual patient characteristics, including tumor growth pattern, degree of hearing loss and vertigo, and patient age, guide optimal management.[3]

The three most common surgical approaches for the resection of vestibular schwannomas are the translabyrinthine, middle fossa, and retrosigmoid approaches. While hearing cannot be preserved through the translabyrinthine approach, the direct access to the IAC and potential benefits in the preservation of facial nerve continuity makes it a favorable proposition for tumors exceeding 3 cm and for smaller tumors with significantly impaired hearing.[4] In addition, the translabyrinthine approach largely avoids cerebellar retraction. The middle fossa and retrosigmoid approaches, on the other hand, carry advantages: the former allows excellent exposure of the IAC for the resection of intracanalicular tumors or tumors with limited cerebellopontine angle (CPA) involvement,[5] [6] whereas the latter can provide a clear view of the facial nerve at the root entry zone as well as the fundus and may be more suited for tumors with a larger CPA component.[7] Ultimately, the decision for surgical approach lies with surgeon preference.

Complications of surgery for vestibular schwannomas include facial nerve paresis or paralysis, hearing loss, cerebrospinal fluid (CSF) leak, and tumor recurrence.[8] Management of recurrent tumors following microsurgical resection depends on symptomatology and documented growth rate, but strong consideration is given to stereotactic radiation and revision surgery.[9] Not surprisingly, revision surgery has been associated with increased complication rates. In this study, we seek to describe our institution's experience with revision surgery for vestibular schwannomas, with particular emphasis placed on the choice of surgical approach and perioperative complications.

Materials and Methods

Patients

This study received Institutional Review Board approval at St. Vincent Medical Center, Los Angeles, California, United States. An internal database of patients undergoing surgery for vestibular schwannomas between January 1985 and June 2015 was reviewed. Inclusion criteria were as follows: surgery performed on the same anatomical side following a history of prior surgery for vestibular schwannoma with an original pathological diagnosis of vestibular schwannoma, at our institution or at any other institution, with or without a diagnosis of neurofibromatosis type 2 (NF2), with or without a history of radiation therapy. Indication for surgery was a growing residual tumor in all cases. Patients with NF2 who underwent one surgery on each side did not meet inclusion criteria for revision surgery and were specifically excluded. Demographic and clinical data were aggregated.

Tumor dimensions were obtained from cross-sectional imaging, and the largest dimension from measurements in three planes—craniocaudal, anteroposterior, and transverse, including any IAC component—was taken as the tumor size.

Factors behind the choice of surgical approach for the revision surgery varied. Patients who had previously undergone a translabyrinthine approach usually underwent a second translabyrinthine approach for the revision surgery. Similarly, patients with no serviceable hearing following the first surgery often underwent a translabyrinthine approach for the revision surgery. However, no strict criteria were used when choosing the specific surgical approach, and the decision for approach was made on a case-by-case basis.

The decision for the extent of resection was generally taken intraoperatively; severe adherence to the brainstem or the facial nerve or lack of a clean plane of dissection led to the intraoperative decision for a partial resection. However, if the tumor was documented at the time of previous surgery to be adherent to the brainstem or the facial nerve, a partial resection was planned preoperatively.

Statistical Analysis

Mann–Whitney U and Kruskal–Wallis tests were employed to compare facial nerve outcomes with patients stratified by various characteristics. The Dunn–Bonferroni test was used as posthoc testing following any significant differences noted with the Kruskal–Wallis test. Statistical analysis was performed with SPSS (IBM, Armonk, New York, United States).

Results

In total, 231 unique patients, 102 males and 129 females, who underwent 250 revision surgeries within the study period were identified, with a mean length to follow-up of 30 days (range: 4 days to 1.75 years). The mean age was 43 years (range: 12–88 years; [Table 1]).

Table 1 Patient characteristics

	Number	Percentage
Gender	103 males	44
	131 females	56
Laterality	125 right	50
	124 left	50
Location of prior surgery	Own institution: 36	14
	Other institution: 197	86
Preoperative irradiation	22	10
Neurofibromatosis type 2	86	37
Surgical approach	Translabyrinthine: 217	87
	Transcochlear: 14	6
	Middle fossa: 13	5
	Retrosigmoid: 6	2
Extent of resection	Gross total: 212	85
	Subtotal: 33	13
	Decompression only: 4	2
Intraoperative transfusion	30	14
Cerebrospinal fluid leak	21	8.4
Ventriculoperitoneal shunt	2	0.8
	Mean	Range
Age (years)	42.9	12–88
Length to follow-up	30 d	4 d to 1.8 y
Number of prior surgeries	1.26	1–4
Size of tumor at surgery (cm)	2.6	0.5–6.9
Operating time (hours)	4.6	1–12
Estimated blood loss (mL)	342	40–3,000

Note: Reported percentages are calculated using number of patients for whom data were available.

The mean number of prior surgeries was 1.26 (range: 1–4). Thirty-six surgeries followed a prior resection at our institution; 197 followed surgeries performed at other institutions. Twenty-two (10%) patients had undergone stereotactic radiation or other radiotherapy before the present surgery. Of the 15 patients who underwent more than one revision surgery at our institution, 9 carried a diagnosis of NF2 whereas 6 did not.

Surgical approaches included the translabyrinthine approach (n = 217, 87%), the transcochlear extension of the translabyrinthine approach (n = 14, 6%), the middle fossa approach (n = 13, 5%), and the retrosigmoid approach (n = 6, 2%). Gross total resection was achieved in 212 surgeries (85%); preoperative planned partial resection was performed in 11 surgeries (4%), whereas an intraoperative decision for partial resection was made in 22 surgeries (9%).

Surgeries lasted an average of 4.6 hours (range: 1–12 hours). Mean tumor size at the time of surgery as 2.6 cm (range: 0.5–6.9 cm). Mean surgical time was 4.6 hours (range: 1–12 hours). Estimated blood loss, on average, was 342 mL (range: 40–3,000 mL). Intraoperative transfusion was performed during 30 surgeries (14%), with a mean transfusion of 1.4 units.

Facial nerve function was analyzed separately for patients with and without a diagnosis of NF2. For non-NF2 patients, the mean preoperative facial nerve function, as graded on the House–Brackmann scale,[10] was 2.7 (range: 1–6). The mean immediate postoperative facial nerve function (defined as facial nerve function within the first 24 hours following surgery) was 3.2 (range: 1–6), and the mean facial nerve function at last follow-up was 3.8 (range: 1–6). For patients with NF2, the mean preoperative facial nerve function was 2.7 (range: 1–6). The mean immediate postoperative facial nerve function was 3.8 (range: 1–6), and the mean facial nerve function at last follow-up was 3.9 (range: 1–6; [Fig. 1] and [Table 2]). When comparing facial nerve function between non-NF2 and NF2 groups, there was no significant difference when comparing preoperative values (p = 0.694; Mann–Whitney U), immediate postoperative values (p = 0.094; Mann–Whitney U), and values at last follow-up (p = 0.625; Mann–Whitney U).

Table 2 Facial nerve function for all patients preoperatively, immediate postoperatively, and at last follow-up (mean duration, 30 days), as graded on the House–Brackmann scale

	Preoperative (%)	Immediate postoperative (%)	Last follow-up (%)
I	108 (43%)	63 (30%)	52 (27%)
II	29 (12%)	23 (11%)	14 (7%)
III	36 (15%)	30 (14%)	24 (12%)
IV	25 (10%)	17 (8%)	12 (6%)
V	9 (4%)	17 (8%)	22 (11%)
VI	40 (16%)	60 (29%)	69 (36%)

Fig. 1 Distribution of facial nerve function (A) preoperatively, (B) immediate postoperatively, and (C) at last follow-up (mean duration, 30 days), as graded on the House–Brackmann scale.

Facial nerve function was further analyzed separately for patients who had a history of radiation therapy preceding the revision surgery and those who did not. There was no significant difference between radiation and nonradiation groups with respect to preoperative facial nerve function (Mann–Whitney U; p = 0.075) as well as postoperative facial nerve function (p = 0.148).

Preoperative facial nerve function did not depend on the extent of resection (p = 0.195; Kruskal–Wallis), but postoperative facial nerve function was significantly different among the extent of resection (p = 0.016). However, posthoc testing (Dunn–Bonferroni) revealed no significant pairwise differences between groups when comparing the extent of resection (p > 0.05 for all).

Preoperative facial function was significantly different among different surgical approaches (p = 0.000; Kruskal–Wallis). Pairwise comparisons revealed that patients undergoing the transcochlear approach had worse preoperative facial nerve function than patients undergoing the middle fossa, retrosigmoid, and translabyrinthine approaches (p = 0.000 for all; Dunn–Bonferroni). Postoperative facial function was also significantly different among different surgical approaches (p = 0.000, Kruskal–Wallis). Pairwise comparisons revealed that patients undergoing the transcochlear approach had worse postoperative facial nerve function than patients undergoing middle fossa and retrosigmoid approaches (p = 0.000 and p = 0.015, respectively, Dunn-Bonferroni), but there was no significant difference between translabyrinthine and transcochlear approaches (p = 0.224; Dunn–Bonferroni).

Twenty-one CSF leaks were encountered (8%); of these, six cases required reoperation. Two (1%) patients required eventual placement of a ventriculoperitoneal shunt. No perioperative mortality was noted.

Pathological analysis of the resection specimen confirmed a diagnosis of vestibular schwannoma in 233 cases (93%); six specimens from revision surgeries were reported as meningiomas (2.4%), whereas pathology was unavailable in 11 cases.

Discussion

While gross total resection is often performed in primary microsurgery for vestibular schwannomas, near-total and subtotal resections may be electively performed if involvement of adjacent structures, such as the facial nerve, is present. While the choice of surgical approach may be correlated with the extent of tumor removal,[11] [12] the extent of resection has been shown to be unrelated to tumor recurrence, which has been estimated at approximately 9% following primary microsurgery.[12] Revision surgery is generally indicated in patients with growing residual or recurrent disease, and planar measurements have been shown to be adequate in trending growth of residual or recurrent tumors.[13]

Previous series on revision surgeries for vestibular schwannomas emphasize the relatively higher rate of complications, including CSF leaks, new cranial nerve deficits, cerebrovascular accidents, and hematomas.[14] Patients with residual or recurrent disease after a prior retrosigmoid approach may be successfully treated with a translabyrinthine or transcochlear approach.[11]

In this descriptive series, a majority of patients (87%) underwent revision surgery through the translabyrinthine approach; a transcochlear approach was employed in an additional 6% of patients. In our experience, the translabyrinthine approach allows for excellent exposure and minimizes cerebellar retraction, and the transcochlear approach, often performed in a canal-wall-down fashion with blind sac closure of the external auditory canal, can provide additional access, particularly to the anterior extent of the tumor.

Unsurprisingly, preoperative and postoperative facial nerve functions were generally poorer than those encountered with primary surgeries, including when compared with a series of translabyrinthine surgeries performed at our own institution.[15] Non-NF2 and NF2 patients did not differ significantly with respect to preoperative facial function, immediate postoperative facial function, or facial function at last follow-up. However, the mean length to follow-up was 30 days, with significant variation, and long-term facial nerve outcomes in this population are difficult to infer.

In this series, the CSF leak rate was 8%. This is comparable to, or even slightly exceeds, published CSF leak rates for all vestibular schwannoma surgeries, which have been reported to range from 0 to 17%,[16] [17] [18] [19] [20] with most series reporting leak rates of approximately 5 to 6%.[15] [21] [22] In our practice, both nasal and incisional CSF leaks following translabyrinthine or transcochlear craniotomy are treated with revision craniotomy, replacement of fat graft packing, and blind sac closure of the external auditory canal. For CSF leaks following middle fossa or retrosigmoid approach, a lumbar drain is the first line of therapy, and ventriculoperitoneal shunts are reserved for patients demonstrating dependence on a lumbar drain to abate the CSF leak.

A significant limitation of this study was the relatively short duration of follow-up for several patients, many of whom were evaluated in person only immediately preceding and several weeks following surgery. Long-term follow-up, particularly of facial nerve function, was therefore not available for many patients, and postoperative facial nerve function, as noted here, may underestimate the rates of recovery of function. Furthermore, neurologic complications and hearing status were not comprehensively documented.

Conclusion

Revision surgery for vestibular schwannomas, where indicated, is feasible and safe, and complication rates, including CSF leak rates, approximate those encountered with primary surgery. Our preferred approach is the translabyrinthine craniotomy, which can be expanded to include the transcochlear approach for greater exposure.

No conflict of interest has been declared by the author(s).

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