Prognostic Impact and Clinical Profile of a Large Cohort of High-Riding Jugular Bulbs in Vestibular Schwannoma Surgery: A Multi-Institutional Analysis over Three Decades
Abstract
Introduction: High-riding jugular bulb (HRJB) is a rare anatomical variant encountered during vestibular schwannoma (VS) surgery which can complicate excision, particularly during drilling of the internal auditory canal (IAC) or internal-auditory-meatus (IAM). Large-scale, multi-institutional data examining patients with HRJB remain scarce. This study addresses this gap through comprehensive analysis from three large tertiary care centers in New-England, over a 35-year period. Objectives: To characterize clinical and demographic features, operative approaches, and postoperative outcomes in patients with HRJB compared with those without, and to evaluate the prognostic significance of HRJB on postoperative complications and functional outcomes. Methods: We retrospectively analyzed 2,139 patients undergoing VS resection from 1990 to 2025 across three tertiary institutions within the MGB system. Patients were stratified by the presence of HRJB ( n = 59) or absence ( n = 2080). Baseline demographics, lesion characteristics, operative approach, laboratory parameters, and postoperative complications were compared. To mitigate inflated type-I error due to multiple testing, no t -tests or chi-square tests were performed. Multivariate logistic regression adjusting for confounders (age, GTR, lesion-size, operative approach, BMI, tobacco history, cystic lesion, nutrition status) was utilized to assess the independent prognostic impact of HRJB. Results: Patients with HRJB were older (mean age 54.12 ± 11.43 years versus 49.50 ± 13.19 years) and predominantly female (72.9% versus 54.9%). Lesion size was larger in the HRJB group (25.30 ± 5.85 mm) compared with controls (23.06 ± 10.24 mm). The majority in both cohorts underwent retrosigmoid craniotomy (76.3% HRJB versus 76.1% non-HRJB). Gross total resection (GTR) was achieved more frequently in HRJB patients (64.4% versus 48.6%), possibly reflecting surgical selection or tumor characteristics. Baseline functional assessments showed a higher proportion of HRJB patients with moderate disability (mRS 3 in 33.9% versus 22.2%) and elevated baseline Barthel scores (61–99 in 37.3% versus 25.0%), indicating a different preoperative status. Postoperatively, the HRJB cohort exhibited increased CSF leak rates (11.9% versus 5.6%) and a higher incidence of peri-tumoral radiographic changes (diffusion restriction, T2 hyperintensity, parenchymal shrinkage, or encephalomalacia, 33.9% versus 23.8%). Hydrocephalus rates were similar between groups (13.6%). Recurrence rates trended lower in the HRJB group (6.8% versus 10.6%), which may correlate with the higher GTR rate. Multivariate logistic regression confirmed that HRJB was an independent risk factor for postoperative CSF leak (Odds Ratio [OR] 12.33; 95% Confidence Interval [CI] 1.55–98.18; p = 0.018). No significant associations were found between HRJB and hydrocephalus (OR 0.69; p = 0.786), radiographic recurrence (OR 0.00; p = 0.999), or poor functional outcome (OR 1.03; p = 0.976). Other confounders accounted for included age, GTR, lesion size, operative approach, BMI, tobacco use, cystic-changes, nutrition status, HRJB. Conclusion: This largest-to-date multi-institutional study elucidates the distinct clinical profile and surgical risks associated with HRJB in VS . Patients with HRJB tend to be older, female, and present with larger tumors. HRJB elevates the risk of postoperative CSF leak. We believe this could be due to an increased risk of mastoid air cell entry, impairment of the surgeon’s ability to create watertight closure along the sigmoid sinus margin, or alterations in venous outflow dynamics/pressures adjacent to the dura. Publication History Article published online: 27 February 2026 © 2026. Thieme. All rights reserved. Georg Thieme Verlag KG Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
Fields of Study & Subjects
Meningioma and schwannoma management
Adrenal and Paraganglionic Tumors
Ear and Head Tumors
Publication details
- Journal / source
- Journal of Neurological Surgery Part B Skull Base
- Volume
- 87
- Issue
- S 01
- Pages
- S1–S548
- Publication date
- 27 February 2026
- Language
- EN