» Articles » PMID: 20192620

Functional Outcome After Resection of Spinal Cord Hemangioblastomas Associated with Von Hippel-Lindau Disease

Overview
Date 2010 Mar 3
PMID 20192620
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Object: Spinal cord hemangioblastomas are a common protean manifestation of von Hippel-Lindau (VHL) disease and can be associated with significant morbidity. To better define expected outcome and optimal management of these tumors in the context of this neoplasia syndrome, the authors analyzed the findings from patients with VHL disease who underwent resection of spinal cord hemangioblastomas.

Methods: Consecutive patients with VHL disease who underwent surgery for spinal cord hemangioblastomas with > 6 months follow-up were included in the study. Serial clinical examinations, functional scores, imaging findings, and operative records were analyzed.

Results: One hundred eight patients (57 male, 51 female) underwent 156 operations for resection of 218 spinal cord hemangioblastomas. One hundred forty-six operations (94%) were performed for symptom-producing tumors. The most common presenting symptoms included hypesthesia (64% of resections), hyperreflexia (57%), dysesthesia (43%), and weakness (36%). Mean follow-up was 7.0 +/- 5.0 years (range 0.5-20.9 years). Complete resection was achieved for 217 tumors (99.5%). At 6-months follow-up, patients were stable or improved after 149 operations (96%) and worse after 7 operations (4%). Ventral tumors (OR 15.66, 95% CI 2.54-96.45; p = 0.003) or completely intramedullary tumors (OR 10.74, 95% CI 2.07-55.66; p = 0.005) were associated with an increased risk of postoperative worsening. The proportion of patients remaining functionally stable at 2, 5, 10, and 15 years' follow-up was 93, 86, 78, and 78%. Long-term functional decline was caused by extensive VHL-associated CNS disease (6 patients), VHL-associated visceral disease (1 patient), or non-VHL disease (2 patients).

Conclusions: Resection of symptomatic spinal cord hemangioblastomas is a safe and effective means of preserving neurological function in patients with VHL disease. Tumor location (ventral or completely intramedullary) can be used to assess functional risk associated with surgery. Long-term decline in neurological function is usually caused by VHL-associated disease progression.

Citing Articles

Spinal cord hemangioblastomas in von Hippel-Lindau disease.

Kreatsoulas D, Lonser R Neurooncol Adv. 2024; 6(Suppl 3):iii66-iii72.

PMID: 39430395 PMC: 11485647. DOI: 10.1093/noajnl/vdad153.


En Bloc Resection for Spinal Cord Hemangioblastomas: Surgical Technique and Clinical Outcomes.

Chen X, Guo H, Zhang J, Ye J, Wang S, Jiang H J Neurol Surg A Cent Eur Neurosurg. 2023; 85(6):577-584.

PMID: 37992732 PMC: 11452231. DOI: 10.1055/s-0043-1776707.


Benign Spinal Tumors.

Noureldine M, Shimony N, Jallo G Adv Exp Med Biol. 2023; 1405:583-606.

PMID: 37452955 DOI: 10.1007/978-3-031-23705-8_23.


Hemangioblastomas and Other Vascular Origating Tumors of Brain or Spinal Cord.

Vetrano I, Gioppo A, Farago G, Pinzi V, Pollo B, Broggi M Adv Exp Med Biol. 2023; 1405:377-403.

PMID: 37452946 DOI: 10.1007/978-3-031-23705-8_14.


Case report: High-resolution, intra-operative µDoppler-imaging of spinal cord hemangioblastoma.

Soloukey S, Verhoef L, Generowicz B, De Zeeuw C, Koekkoek S, Vincent A Front Surg. 2023; 10:1153605.

PMID: 37342792 PMC: 10277559. DOI: 10.3389/fsurg.2023.1153605.