Abstract
Background
Hemifacial spasm is usually caused by arterial compression at the root exit zone of the facial nerve. However, other etiologies have been reported. The aim of this study was to analyze the frequency of other causes of hemifacial spasm.
Methods
Our prospectively maintained hemifacial spasm database containing all patients who underwent microvascular decompression (MVD) for hemifacial spasm from 2002 to 2018 was reviewed. All offending structures were identified and recorded by the surgeon at the time of surgery. Additionally, the operative videos were analyzed retrospectively.
Results
MVD was performed in 353 patients. Arterial compression was the main cause of hemifacial spasm in 341 (96.9%) patients. Combined venous-arterial compression was seen in 7 (2.0%) patients. In one patient, the compression was from a large vein. In two patients, no compression was found. One patient who suffered from Bell’s palsy many years previously had severe synkinesis and the other had facial tics. In two patients, the spasm was caused due to strangulation of the facial nerve by arachnoid bands. Long-term follow-up of more than 18 months was available in 249 patients with total resolution or near total resolution of spasms in 89.96% of patients.
Conclusions
In most patients with hemifacial spasm, arterial vessels are involved in compressing the facial nerve. Purely venous compression is rarely encountered. We report for the very first time arachnoid bands strangulating the nerve as a cause for hemifacial spasm without involvement of any vessel.
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Introduction
Hemifacial spasm is characterized by progressive, involuntary, irregular, clonic or tonic movement of the muscles innervated by the facial nerve [31]. In most cases, the etiology is attributed to arterial compression at the root exit zone of the facial nerve. However, other etiologies that may cause hemifacial spasm have been reported [32]. Hemifacial spasm can occur due to other rare causes including all kinds of space-occupying lesions in the cerebellopontine angle. In addition, certain processes in the brainstem can also result in symptoms. These include gliomas, demyelinating neurological disorders such as multiple sclerosis or brainstem infarction [26, 31, 32].
In this study, we analyzed data from our database in order to identify the etiology of hemifacial spasm.
Methods
Data collection
The local ethics committee approved this retrospective study. Our prospectively maintained hemifacial spasm database containing all patients who underwent microvascular decompression (MVD) for hemifacial spasm from 2002 to 2018 was retrospectively reviewed regarding the cause for facial nerve root compression and outcome. Patient data were prospectively collected including preoperative clinical picture, magnetic resonance (MR) imaging findings, operative notes, intraoperative videos, and postoperative outcome at last follow-up. Additionally, the operative videos were analyzed retrospectively to confirm the intraoperative findings. Routine follow-up was done both by outpatient visits and telephone calls. The compression of the facial nerve was assessed radiologically and confirmed intraoperatively by endoscopic visualization of the facial nerve root exit zone (REZ). Etiological factors were identified and analyzed.
Subgroup analysis regarding outcome was performed based on cause of hemifacial spasm. The outcome was divided into 4 grades: (1) excellent (hemifacial spasm absent), (2) good (hemifacial spasm> 90% resolved), (3) fair (hemifacial spasm 90-50% resolved), and (4) poor (hemifacial spasm< 50% resolved). Ninety percent improvement means that no visible spasms occurred or rarely slight spasms were observed that did not occur daily.
Operative technique
All surgeries were performed via an inferior retrosigmoid approach in the supine position under brainstem auditory evoked potentials and facial electromyography monitoring [9, 10]. An endoscope-assisted microscopic technique as described elsewhere was applied [11, 25]. The endoscope was used to inspect the course of the facial nerve from the pontomedullary sulcus to the entrance into the internal auditory canal. Decompression was achieved by interposing shredded Teflon or by transposing the vessel with a Teflon or Gortex sling which was fixed to the basal dura with a suture or aneurysm clip. All MVDs were performed by the senior author (HWSS) who prospectively recorded the compression pattern at the time of surgery.
Results
Patient demographics
A total of 353 patients suffering from hemifacial spasm underwent MVD in our institution from 2002 to 2018. We offered surgery for all patients even when the symptoms were mild, but the patients felt uncomfortable. Some patients were suffering tremendously even from mild spasms. However, most patients had severe functionally impairing spasms. The only exclusion criteria was a high risk for general anesthesia because of comorbidity. There were 136 (38.5%) male and 217 (61.5%) female patients. The symptoms were left-sided in 211 and right-sided in 142 patients. The mean age was 54.78 years ranging from 22 to 81 years. The mean duration of the spasms was 7.78 years ranging from less than 1 to 35 years. Mean follow-up was 51.64 months ranging from 0 to 194 months.
In 249 patients with a follow-up of at least 18 months, the cause of compression and degree of improvement were analyzed.
Compression pattern and outcome
The causes of compression in all patients were collected in Table 1. Additionally, we had one patient with hemifacial spasm caused by an epidermoid who was excluded from the study because no MVD was performed, but a tumor resection which resulted in complete resolution of the spasms. Arterial compression was the main cause of hemifacial spasm in 341 (96.6%) patients with different combinations of vessels. The most frequent offending vessel was posterior inferior cerebellar artery (PICA) (122, 34.6%) followed by anterior inferior cerebellar artery (AICA) (90, 25.5%) and VA (11, 3.12%). Complex arterial compression was seen in 118 patients. The most frequently observed complex compression was a combination of AICA + VA (41, 11.6%) followed by PICA + VA (38, 10.8%), AICA + PICA (26, 7.37%), AICA + PICA + VA (12, 3.4%), and AICA + BA (1, 0.28%). The outcome in the arterial compression group in patients with at least one and half year follow-up (n = 240) was excellent, good, fair, and poor in 194 (80, 83%), 24 (10.0%), 18 (7.50%), and 4 (1.66%) respectively. PICA was the most common cause of compression in 83 patients, where total resolution occurred in 66 patients and near total resolution in 8 patients.
Combined venous-arterial “sandwich” compression was detected in seven (2.0%) patients. A vein was compressing the facial nerve together with AICA and PICA in four (1.1%) and three (0.9%) patients respectively. In one patient, the vein was located above the facial nerve. In six cases, the vein was located between brainstem and facial nerve running between facial and vestibulocochlear nerve down to the pontomedullary sulcus. Because of this unfavorable course, the veins could not be decompressed sufficiently. All attempts to mobilize these veins failed. Furthermore, we did not coagulate the veins because of the unpredictable sequelae. Only in one patient, a little piece of shredded Teflon could be interposed between facial nerve and vein. This patient is without spasms 59 months after surgery. In all other patients, only the arteries were mobilized and decompressed (Fig. 1). Three patients had an excellent and one patient a good outcome (follow-up 33–71 months). In two patients with a large vein running between facial nerve and brainstem where the vein was flattening the facial nerve at the REZ, the outcome was fair and poor respectively. The patient with the poor outcome had additionally a very narrow cistern (Fig. 2). The AICA was decompressed, but he still needs botox injections to control the spasm 98 months after surgery. The other patient improved after PICA decompression and had a fair outcome after 71 months follow-up (Fig. 3).
A purely venous compression was seen in one patient only. It was a large vein, running between facial and vestibulocochlear nerve down to the pontomedullary sulcus. Together with its side branch, it compressed the facial nerve (Fig. 4a). After separating the vein from the facial nerve, a flattening of the nerve was clearly seen (Fig. 4b). The facial nerve was decompressed by transposing the vein laterally with the aid of a Teflon sling which was fixed with a stitch to the dura between jugular foramen and internal auditory canal (Fig. 4c). The patient had been spasm-free immediately after the surgery (follow-up 88 months).
No compression was found in two patients. One patient did not mention to us that he had facial palsy (Bell’s palsy) several years previously. The spasms looked very similar to hemifacial spasm, but were obviously synkinesis after facial nerve damage. Not surprisingly, he did not improve. The other patient was misdiagnosed as hemifacial spasm and after surgery it was proven to be facial tics which were verified by absence of lateral spreads. She did not improve as well.
In two (0.6%) patients, the hemifacial spasm was caused by an unusual strangulation of the facial nerve at the REZ by arachnoid bands. Endoscopic inspection with a 45° endoscope confirmed that there was no vascular compression. In neither case was there a history of meningitis, head injury, or hemorrhage. The first patient was a 41-year-old male who had complained of hemifacial spasm for 10 years. He presented with a slight facial palsy (HB 2) because of previous botulinum toxin injections. Time-of-Flight (TOF) and Constructive interference in steady state (CISS) MR imaging revealed no vascular compression (Fig. 5a, b). Surgical exploration showed a small vein running close to the facial REZ above the nerve and a small arteriole, but these vessels did not cause any compression However, a little bit more distally a clear strangulation of the facial nerve by several arachnoid bands became apparent. (Fig. 5c, d). The arachnoid bands were cut with microscissors to release the nerve (Fig. 5e, f). Immediately after surgery the spasm disappeared. The patient had no complaints 26 months after surgery.
The second patient was a 32-year-old male who had suffered from hemifacial spasm for 20 years. TOF and CISS MR imaging showed no vascular compression, but an asymmetry of the facial nerve when compared with the other side (Fig. 6a, b). The left facial nerve seemed to be anteriorly displaced. Endoscopic inspection revealed a severe strangulation of the facial nerve by arachnoid bands (Fig. 6c). On the dorsal side of the nerve, an unusual gliotic band was identified which seemed to pull the nerve anteriorly (Fig. 6d). The bands and the fibrotic perineurium were cut. Careful elevation of the nerve showed significant damage of the nerve at the area of the former strangulation (Fig. 6e). The final inspection showed the released nerve (Fig. 6f). The patient was spasm-free immediately after surgery. Nine days later, he developed a delayed facial palsy (HB 6). Fortunately, the palsy resolved completely 50 day after surgery. He was doing well without spasms 15 months after surgery.
Overall outcome
The overall outcome of 249 patients with a minimum follow-up of 18 months is shown in Table 2. 198 (79.52%) patients were spasm-free. A total of 26 (10.44%) patients had a good and 19 (7.63%) a fair outcome. In 6 (2.41%) patients, we observed a poor outcome. The reason for a poor outcome was mostly a structural damage of the facial nerve due to prolonged severe compression by elongated vessels and in one patient mentioned above a combination of severe venous compression.
Long-term outcome according to type of compression
The range of improvement according to different types of compression is shown in Table 2. In arterial compression, the best long-term outcome occurred after MVD of complex AICA-PICA compression with total resolution of spasms in 94.44% of patients (17 out of 18 patient), and the worst outcome in the combination of AICA and vein with 66.67% of patients experienced at least 90% improvement with no spasm free patients in this group.
Discussion
Summary of the key results
Our study shows that although arterial compression is usually the cause of hemifacial spasm, other very rare causes exist [5, 19, 21, 23, 26]. To the best of our knowledge, we report for the first time cases of hemifacial spasm caused by arachnoid bands which strangulated the facial nerve at the REZ. After simply cutting the arachnoid bands, the spasms disappeared in both patients. Pure venous compression is also exceedingly rare. The compression pattern is very variable in hemifacial spasm. The most frequent offending vessel is PICA followed by AICA, but often a complex compression is encountered with a combination of two or three vessels.
Venous compression
Venous compression was reported in most of the large clinical studies [3, 16, 28, 33]. Purely venous compression in hemifacial spasm is rare. In a recent review by Dumot and Sindou, an incidence of 0.1% was given [8]. Han et al. found 5 (0.3%) patients with venous compression in their series of 1642 patients [13] that is in accordance with our series. We saw just one venous compression (0.28%) in our series of 353 patients, but we can confirm that a vein can cause symptomatic compression of the facial nerve. We had an excellent outcome in this patient after transposing the vein with a Teflon sling. However, more frequently venous compression is accompanied by arterial compression, which we saw in seven patients. Typically, there was a sandwich compression with the facial nerve in between vein and artery. In six of these seven patients, only the artery was decompressed which resulted in excellent outcome in three and good outcome in one patient confirming that the artery was the main spasm-causing offender and not the vein. However, in two patients, the outcome was less favorable. In one patient, who had a poor outcome, the facial nerve was compressed at the REZ by a large vein and an AICA loop. The AICA was transposed anteriorly and fixed with shredded Teflon which was placed between brainstem and skull base. In this patient, the brainstem was almost in contact with the skull base due to a very narrow prepontine cistern, which was probably the reason for the failure of our decompression. In the other patient, who had a fair outcome (60% improvement), the PICA was decompressed, but there was a large vein which stretched the facial REZ. Because of the course of the vein, dissection and mobilization of the vein was not possible. There were several small side branches draining the brainstem into this vein. Therefore, we did not dare to coagulate it because of the unpredictable sequelae.
Some authors reported the need of decompression of the facial nerve from the compression exerted by a vein, even if the vein has to be coagulated and cut [13, 19]. Although the complications which could occur from venous sacrifice along the cerebellopontine angle seem to be rare, there is still a risk of venous congestion and infarction that made our surgical preference not to sacrifice these kinds of veins [8, 22].
Arachnoid strangulation of the facial nerve
We report a rare cause of hemifacial spasm that to our knowledge has not previously been described in the literature. In two patients, the facial nerve was found strangulated by arachnoid bands without any vascular compression. In both patients, the spasm immediately disappeared simply after cutting the arachnoid bands and, in one patient, additionally the fibrotic perineurium. Although hemifacial spasm due to arachnoid cysts within the cerebellopontine angle is described, strangulation of the facial nerve by arachnoid bands has not been reported.
The etiology of the arachnoid bands remains unclear. There was no history of trauma, hemorrhage, or infection in both patients. In the second patient in whom the spasms started at the age of 12, there was obviously a congenital abnormality. The facial nerve seemed to be tethered by a gliotic band which contributed to the severe strangulation. MR imaging clearly showed anterior displacement of the facial nerve at the brain stem.
Space-occupying lesion-related hemifacial spasm
A variety of rare causes of hemifacial spasm have been previously reported in the literature [12, 14, 18, 27]. Most of these were epidermoid tumors [1, 6, 7, 17] or arachnoid cysts [4, 15, 18, 24, 27, 30]. The incidence of hemifacial spasm caused by a tumor is reported as 0.3 to 2.5% [2, 20, 29]. We have seen only one patient with epidermoid-induced hemifacial spasm, who was free of symptoms after resection. This patient was not included in this series because only MVD was evaluated but not tumor surgeries.
Absence of compression
A few authors stated that most patients with hemifacial spasm had no apparent etiology [31]. However, our data clearly show that this statement is not true. In all our patients with hemifacial spasm, we found a morphological structure which was responsible for the spasm. Both patients without compression were misdiagnosed by us. One patient presented with severe synkinesis after Bell’s palsy, the other with facial tics. MR imaging showed in both cases a close relationship between AICA and facial nerve, but the endoscopic inspection revealed no contact at all. It had been reported that peripheral facial nerve injury or Bell’s palsy can result in hemifacial spasm [31]. However, in our opinion, that is not correct. Facial nerve lesions may lead to synkinesis. But synkinesis occurs during voluntary movements, but not or very spontaneously. Facial tics can be interrupted voluntarily, while hemifacial spasms cannot. Electrophysiology has been helpful in differentiating these conditions from hemifacial spasms by documenting either lack of lateral spread or electrophysiological evidence of old facial nerve injury and synkinesis [28, 31].
Conclusions
In most patients with hemifacial spasm, arterial vessels are involved in compressing the facial nerve REZ at the brain stem. Purely venous compression is rarely encountered. This is the first report of arachnoid bands strangulating the nerve as a cause for hemifacial spasm without involvement of any vessel.
References
Alemdar M (2012) Epidermoid cyst causing hemifacial spasm epidermoid cyst in cerebellopontine angle presenting with hemifacial spasm. J Neurosci Rural Pract 3(3):344–346
Auger RG, Piepgras DG (1989) Hemifacial spasm associated with epidermoid tumors of the cerebellopontine angle. Neurology 39(4):577–580
Barker FG, Jannetta PJ, Bissonette DJ, Shields PT, Larkins MV, Jho HD (1995) Microvascular decompression for hemifacial spasm. J Neurosurg:201–210
Bonde V, Muzumdar D, Goel A (2008) Retroclival arachnoid cyst with hemifacial spasm. Singap Med J 49(10):e281–e282
Campos-Benitez M, Kaufmann AM (2008) Neurovascular compression findings in hemifacial spasm. J Neurosurg 109(3):416–420
Choi S-K, Rhee B-A, Lim YJ (2009) Hemifacial spasm caused by epidermoid tumor at cerebello pontine angle. J Korean Neurosurg Soc 45(3):196–198
Desai K, Nadkarni T, Bhayani R, Goel A (2003) Cerebellopontine angle epidermoid tumor presenting with hemifacial spasms. Neurol India 51(2):288–289
Dumot C, Sindou M (2018) Veins of the cerebellopontine angle and specific complications of sacrifice, with special emphasis on microvascular decompression surgery. A review. World Neurosurg 117:422–432
El Damaty A, Rosenstengel C, Matthes M, Baldauf J, Schroeder HWS (2016) The value of lateral spread response monitoring in predicting the clinical outcome after microvascular decompression in hemifacial spasm: a prospective study on 100 patients. Neurosurg Rev 39(3):455–466
El Damaty A, Rosenstengel C, Matthes M, Baldauf J, Dziemba O, Hosemann W, Schroeder HWS (2017) A new score to predict the risk of hearing impairment after microvascular decompression for hemifacial spasm. Neurosurgery. https://doi.org/10.1093/neuros/nyx111
El Refaee E, Langner S, Baldauf J, Matthes M, Kirsch M, Schroeder HWS (2013) Value of 3-dimensional high-resolution magnetic resonance imaging in detecting the offending vessel in hemifacial spasm: comparison with intraoperative high definition endoscopic visualization. Neurosurgery 73(1):58–67 discussion 67
Elgamal EA, Coakham HB (2005) Hemifacial spasm caused by pontine glioma: case report and review of the literature. Neurosurg Rev 28(4):330–332
Han I-B, Chang JH, Chang JW, Huh R, Chung SS (2009) Unusual causes and presentations of hemifacial spasm. Neurosurgery 65(1):130–137
Hertz R, Espinosa J, Lucerna A, Stranges D (2017) Multiple sclerosis presenting with facial twitching (myokymia and hemifacial spasms). Case Rep Neurol Med 2017:7180560
Higashi S, Yamashita J, Yamamoto Y, Izumi K (1992) Hemifacial spasm associated with a cerebellopontine angle arachnoid cyst in a young adult. Surg Neurol 37(4):289–292
Huang CI, Chen IH, Lee LS (1992) Microvascular decompression for hemifacial spasm: analyses of operative findings and results in 310 patients. Neurosurgery 30(1):53–56 discussion 56–7
Liu J, Liu P, Zuo Y, Xu X, Liu H, Du R, Yu Y, Yuan Y (2018) Hemifacial spasm as rare clinical presentation of vestibular schwannomas. World Neurosurg 116:e889–e894
Mastronardi L, Taniguchi R, Caroli M, Crispo F, Ferrante L, Fukushima T (2009) Cerebellopontine angle arachnoid cyst: a case of hemifacial spasm caused by an organic lesion other than neurovascular compression: case report. Neurosurgery 65(6):E1205 discussion E1205
Mercier P, Sindou M (2018) The conflicting vessels in hemifacial spasm: literature review and anatomical-surgical implications. Neurochirurgie 64(2):94–100
Miyazaki S, Fukushima T, Nagai A, Tamagawa T (1987) CP angle meningioma presenting as hemifacial spasm. No Shinkei Geka 15(6):683–686
Møller AR (1999) Vascular compression of cranial nerves: II: pathophysiology. Neurol Res 21(5):439–443
Narayan V, Savardekar AR, Patra DP, Mohammed N, Thakur JD, Riaz M, Nanda A (2018) Safety profile of superior petrosal vein (the vein of Dandy) sacrifice in neurosurgical procedures: a systematic review. Neurosurg Focus 45(1):E3
Nielsen VK (1985) Electrophysiology of the facial nerve in hemifacial spasm: ectopic/ephaptic excitation. Muscle Nerve 8(7):545–555
Ogawa H, Hiroshima S, Kamada K (2015) A case of facial spasm associated with ipsilateral cerebellopontine angle arachnoid cyst. Surg J (N Y) 1(1):e38–e40
Refaee EE, El Refaee E, Rosenstengel C, Baldauf J, Pillich DT, Matthes M, Schroeder HWS (2017) Microvascular decompression for patients with hemifacial spasm associated with common trunk anomaly of the cerebellar arteries—case study and review of literature. Oper Neurosurg 14(2):121–127
Rosenstengel C, Matthes M, Baldauf J, Fleck S, Schroeder H (2012) Hemifacial spasm: conservative and surgical treatment options. Dtsch Arztebl Int 109(41):667–673
Ruiz-Juretschke F, Vargas A, González-Rodrigalvarez R, Garcia-Leal R (2015) Hemifacial spasm caused by a cerebellopontine angle arachnoid cyst. Case report and literature review. Neurocirugia 26(6):307–310
Samii M, Günther T, Iaconetta G, Muehling M, Vorkapic P, Samii A (2002) Microvascular decompression to treat hemifacial spasm: long-term results for a consecutive series of 143 patients. Neurosurgery 50(4):712–718 discussion 718–9
Sprik C, Wirtschafter JD (1988) Hemifacial spasm due to intracranial tumor. An international survey of botulinum toxin investigators. Ophthalmology 95(8):1042–1045
Takano S, Maruno T, Shirai S, Nose T (1998) Facial spasm and paroxysmal tinnitus associated with an arachnoid cyst of the cerebellopontine angle--case report. Neurol Med Chir 38(2):100–103
Wang A, Jankovic J (1998) Hemifacial spasm: clinical findings and treatment. Muscle Nerve 21(12):1740–1747
Yaltho TC, Jankovic J (2011) The many faces of hemifacial spasm: differential diagnosis of unilateral facial spasms. Mov Disord 26(9):1582–1592
Zhong J, Zhu J, Sun H, Dou N-N, Wang Y-N, Ying T-T, Xia L, Liu M-X, Tao B-B, Li S-T (2014) Microvascular decompression surgery: surgical principles and technical nuances based on 4000 cases. Neurol Res 36(10):882–893
Acknowledgments
The authors thank Mr Alistair Jenkins for the revision of the study and Mr. Marc Matthes for the technical assistance.
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Henry W. S Schroeder is consultant to Karl Storz GmbH & Co. KG, Tuttlingen, Germany. The rest of the authors declare that they have no conflict of interest.
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El Refaee, E., Marx, S., Rosenstengel, C. et al. Arachnoid bands and venous compression as rare causes of hemifacial spasm: analysis of etiology in 353 patients. Acta Neurochir 162, 211–219 (2020). https://doi.org/10.1007/s00701-019-04119-5
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DOI: https://doi.org/10.1007/s00701-019-04119-5