Technical considerations and long-term results of endovascular venous stenting to control venous hypertension from meningiomas invading intracranial venous sinuses.

cranial venous outflow obstruction endovascular neurosurgery idiopathic intracranial hypertension meningioma papilledema venous sinus stenting

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
08 Sep 2023
Historique:
received: 21 03 2023
accepted: 26 06 2023
pubmed: 19 9 2023
medline: 19 9 2023
entrez: 19 9 2023
Statut: aheadofprint

Résumé

Meningiomas invading the intracranial venous sinuses may cause intracranial venous hypertension, papilledema, and visual compromise. Sinus resection and graft reconstructions, however, add significant complexity to tumor surgery, with the potential for increased morbidity. In this study, the authors explored whether venous sinus stenting might provide an alternative means of controlling venous hypertension that would be sustainable over the long term. The authors performed a retrospective review of all 16 patients with intracranial meningiomas who underwent stenting at their institution for venous sinus compromise. At presentation, all had headache and 9 had papilledema. Thirteen patients had 1 meningioma and 3 had 2 or more. Three patients had had previous tumor resection and radiotherapy. One patient had been treated with a lumboperitoneal shunt and radiotherapy. The median length of clinical follow-up was 8 years (range 4 months-18 years). Venous sinus narrowing was often not confined to the site of meningioma, and bilateral transverse sinus narrowing, reminiscent of that seen in idiopathic intracranial hypertension, was present in 7 patients with sagittal sinus meningiomas. Eleven patients had stents placed solely across sinus narrowing caused by meningioma. Five patients had additional stents placed at other sites of venous narrowing at the same time: in one of these patients, a stent was placed across a defect in the sagittal sinus caused by previous surgery, and in the 4 other patients, stents were placed across nontumor narrowings of the transverse sinuses. In 1 patient, the jugular vein was also stented. Nine patients developed symptomatic in-stent restenosis at the meningioma site. Eight had further stenting procedures with variable success in restoring the in-stent lumen. The remaining patient, with a late partial relapse, is being reinvestigated. Papilledema resolved in all patients after stenting. Six patients experienced prolonged and very substantial relief of all symptoms. Five patients had persistent headache despite restoration of the sinus lumen. Five had persistent symptoms associated with resistant in-stent stenosis. There were no significant complications from any of the diagnostic or therapeutic procedures. In patients who are symptomatic with meningiomas obstructing the venous sinuses, successful stenting of the affected segment can give a good outcome, especially in terms of relieving papilledema. However, further procedures are often necessary to maintain stent patency, other areas of venous compromise frequently coexist, and some patients remain symptomatic despite apparently successful treatment of the index lesion. Long-term surveillance is a requirement.

Identifiants

pubmed: 37724796
doi: 10.3171/2023.6.JNS23607
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-13

Auteurs

J Nicholas P Higgins (JNP)

Departments of1Radiology.

Sherif R W Kirollos (SRW)

2Radiology Department, Queen Elizabeth University Hospital, Birmingham.

Adel Helmy (A)

3Department of Clinical Neurosciences, Division of Neurosurgery, Cambridge University Hospitals, Cambridge, United Kingdom; and.

Mathew R Guilfoyle (MR)

3Department of Clinical Neurosciences, Division of Neurosurgery, Cambridge University Hospitals, Cambridge, United Kingdom; and.

John D Pickard (JD)

3Department of Clinical Neurosciences, Division of Neurosurgery, Cambridge University Hospitals, Cambridge, United Kingdom; and.

Patrick R Axon (PR)

4Skull Base Surgery, and.

Alexis J Joannides (AJ)

3Department of Clinical Neurosciences, Division of Neurosurgery, Cambridge University Hospitals, Cambridge, United Kingdom; and.

Sarah Jefferies (S)

5Oncology, Cambridge University Hospitals, Cambridge.

Thomas Santarius (T)

3Department of Clinical Neurosciences, Division of Neurosurgery, Cambridge University Hospitals, Cambridge, United Kingdom; and.

Ramez Kirollos (R)

6National Neuroscience Institute, Singapore & Dukes-NUS Medical School, Singapore.

Classifications MeSH