Abstract
Abstract
Purpose
Intradural spinal hemangioblastomas are rare highly hypervascularized benign neoplasms. Surgical resection remains the treatment of choice, with a significant risk of postoperative neurological deterioration. Due to the tumor infrequency, scientific evidence is scarce and limited to case reports and small case series.
Methods
We performed a retrospective multicenter study including five high-volume neurosurgical centers analyzing patients surgically treated for spinal hemangioblastomas between 2006 and 2021. We assessed clinical status, surgical data, preoperative angiograms, and embolization when available. Follow-up records were analyzed, and logistic regression performed to assess possible risk factors for neurological deterioration.
Results
We included 60 patients in Germany and Austria. Preoperative angiography was performed in 30% of the cases; 10% of the patients underwent preoperative embolization. Posterior tumor location and presence of a syrinx favored gross total tumor resection (93.8% vs. 83.3% and 97.1% vs. 84%). Preoperative embolization was not associated with postoperative worsening. The clinical outcome revealed a transient postoperative neurological deterioration in 38.3%, depending on symptom duration and preoperative modified McCormick grading, but patients recovered in most cases until follow-up.
Conclusion
Spinal hemangioblastoma patients significantly benefit from early surgical treatment with only transient postoperative deterioration and complete recovery until follow-up. The performance of preoperative angiograms remains subject to center disparities.
Funder
Technische Universität München
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Neurology (clinical),Neurology,Oncology
Reference20 articles.
1. Sadashivam S, Abraham M, Kesavapisharady K, Nair SN (2020) Long-term outcome and prognostic factors of intramedullary spinal hemangioblastomas. Neurosurg Rev 43:169–175. https://doi.org/10.1007/s10143-018-1025-2
2. Deng X, Wang K, Wu L, Yang C, Yang T, Zhao L, Yang J, Wang G, Fang J, Xu Y (2014) Intraspinal hemangioblastomas: analysis of 92 cases in a single institution: clinical article. J Neurosurg Spine 21:260–269. https://doi.org/10.3171/2014.1.SPINE13866
3. Roonprapunt C, Silvera VM, Setton A, Freed D, Epstein FJ, Jallo GI (2001) Surgical management of isolated hemangioblastomas of the spinal cord. Neurosurgery 49:321–327. https://doi.org/10.1097/00006123-200108000-00012. (discussion 327–328)
4. Kanno H, Yamamoto I, Nishikawa R, Matsutani M, Wakabayashi T, Yoshida J, Shitara N, Yamasaki I, Shuin T, Clinical VHLRGiJ (2009) Spinal cord hemangioblastomas in von Hippel-Lindau disease. Spinal Cord 47:447–452. https://doi.org/10.1038/sc.2008.151
5. Djindjian R, Hurth M, Houdart R (1971) Spinal cord hemangioblastomas and von Hippel-Lindau disease (preliminary report apropos of 14 cases studied by spinal cord angiography). Rev Neurol (Paris) 124:495–511
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