Abstract
Background
Spinal arachnoid cysts (SAC) are rare mostly idiopathic intradural lesions with compression of the spinal cord and clinical signs of radiculo- and/or myelopathy. We retrospectively analyzed radiological and clinical characteristics of patients with surgical treatment of SAC including a subgroup evaluation of long-term outcome and QoL.
Method
Patients with SAC treated between 1993 and 2017 were evaluated. Craniocaudal (c.c.) and anteroposterior (a.p) cyst diameters were measured pre- and post-OP. McCormick and Odom score for myelopathy, general outcome and QoL (SF-36, EORTC-QLQ30) were recorded.
Results
A total of 72 patients (female:male = 1.9:1) were analyzed with mean FU of 44.8 ± 60 months (long-term data from 25 patients with FU 78.2 ± 63.9 months). All had surgery due to solitary cysts: 10 cervical (13.9%), 45 thoracic (62.5%), and 17 lumbosacral (23.6%), the majority (79.2%) located dorsally. Main symptoms were gait disturbance (80%), dysesthesia (64%) and paresis (80%). Patients had (hemi-)laminectomy with cyst fenestration in 48 (66.7%) and complete resection in 18 cases (25.0%). Four cases (5.5%) were treated by cystoperitoneal shunt, 2 by marsupialization (2.8%). In total, 11 revisions were necessary in 9/72 (12.5%) patients (one patient underwent 3 revisions). Two patients were reoperated for wound revision/epidural hematoma (each n = 1). Seven patients needed additional cyst wall resection after 1.5–31.0 months due to insufficient cyst shrinking and persistent clinical symptoms after first surgery; most of the cysts were multiple septated and of post-hemorrhagic origin. The mean c.c. size decreased from 5.2 ± 3.7 cm pre-OP to 2.7 ± 3.9 cm (p < 0.05); the a.p. diameter decreased from 1.0 ± 0.5 cm to 0.3 ± 0.3 cm (p < 0.0001) without significant differences between fenestration and resection. McCormick and Odom scores revealed improved symptoms, particularly of gait disturbance, sensory deficits, and general performance. Long-term FU displayed satisfying QoL performance without differences of fenestration or resection.
Conclusion
SAC mostly affect women and are predominantly located in the thoracic spine, becoming apparent with clinical myelopathy. For cysts without intracystic septae and compartments, both fenestration and resection of the cyst wall provided significant reduction of cyst size and clinical improvement.
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Schmutzer et al. present a large series of spinal intradural extramedullary arachnoid cysts. A few aspects are interesting and should be pointed out. First, CISS-3D MRI sequences are valuable in defining a cyst as monocompartimental and, if so, fenestration seems to be as good as cyst wall resection. Second, among the various myelopathic symptoms, only gait ataxia appears to benefit substantially from the surgical treatment. For other symptoms surgery is less beneficial and patients should also be informed on the possibility of relapse over time. Third, post-hemorrhagic cysts are rare but more prone to require revision surgery.
Francesco Sala
Verona, Italy
The authors report on 72 patients who had spinal intradural extramedullary arachnoid cysts. These cysts were treated with either fenestration or resection of the cyst. In a few cases, a cystoperitoneal shunt was utilized, and two patients had marsupialization. Good follow-up was provided with good neurological recovery. A good review of the literature is also provided. The authors found that comparing the two surgical techniques, the results were similar. It is still unclear to this reviewer when fenestration should be done vs. complete resection of the cyst wall. I congratulate the authors on an excellent follow-up when reporting on this relatively rare entity.
Volker K. H. Sonntag
Phoenix, Arizona
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Schmutzer, M., Tonn, JC. & Zausinger, S. Spinal intradural extramedullary arachnoid cysts in adults—operative therapy and clinical outcome. Acta Neurochir 162, 691–702 (2020). https://doi.org/10.1007/s00701-019-04156-0
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DOI: https://doi.org/10.1007/s00701-019-04156-0