Intracranial hypertension induced by internal jugular vein stenosis can be resolved by stenting
D. Zhou
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorCorresponding Author
R. Meng
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Correspondence: R. Meng and X. Ji, Xuanwu Hospital, Capital Medical University, Beijing 100053, China (tel.: +86 10 83198952; fax: +86 10 83154745; e-mail: [email protected] and [email protected]).Search for more papers by this authorX. Zhang
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorL. Guo
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorS. Li
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorW. Wu
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorJ. Duan
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorH. Song
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorY. Ding
Beijing Institute for Brain Disorders, Beijing, China
Department of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA
Search for more papers by this authorCorresponding Author
X. Ji
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Correspondence: R. Meng and X. Ji, Xuanwu Hospital, Capital Medical University, Beijing 100053, China (tel.: +86 10 83198952; fax: +86 10 83154745; e-mail: [email protected] and [email protected]).Search for more papers by this authorD. Zhou
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorCorresponding Author
R. Meng
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Correspondence: R. Meng and X. Ji, Xuanwu Hospital, Capital Medical University, Beijing 100053, China (tel.: +86 10 83198952; fax: +86 10 83154745; e-mail: [email protected] and [email protected]).Search for more papers by this authorX. Zhang
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorL. Guo
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorS. Li
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorW. Wu
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorJ. Duan
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorH. Song
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Search for more papers by this authorY. Ding
Beijing Institute for Brain Disorders, Beijing, China
Department of Neurosurgery, Wayne State University School of Medicine, Detroit, MI, USA
Search for more papers by this authorCorresponding Author
X. Ji
Departments of Neurology, Neurosurgery, and Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China
Beijing Institute for Brain Disorders, Beijing, China
Correspondence: R. Meng and X. Ji, Xuanwu Hospital, Capital Medical University, Beijing 100053, China (tel.: +86 10 83198952; fax: +86 10 83154745; e-mail: [email protected] and [email protected]).Search for more papers by this authorAbstract
Background and purpose
Idiopathic intracranial hypertension (IIH) is characterized by abnormally elevated intracranial pressure (ICP) without identifiable etiology. Recently, however, a subset of patients with presumed IIH have been found with isolated internal jugular vein (IJV) stenosis in the absence of intracranial abnormalities.
Methods
Fifteen consecutive patients were screened from 46 patients suspected as IIH and were finally confirmed as isolated IJV stenosis. The stenotic IJV was corrected with stenting when the trans-stenotic mean pressure gradient (∆MPG) was equal to or higher than 5.44 cmH2O. Dynamic magnetic resonance venography, computed tomographic venography and digital subtraction angiography of the IJV, ∆MPG, ICP, Headache Impact Test 6 and the Frisén papilledema grade score before and after stenting were compared.
Results
All the stenotic IJVs were corrected by stenting. ∆MPG decreased and the abnormal collateral veins disappeared or shrank immediately. Headache, tinnitus, papilledema and ICP were significantly ameliorated at 14 ± 3 days of follow-up (all P < 0.01). At 12 ± 5.6 months of outpatient follow-up, headache disappeared in 14 out of 15 patients (93.3%), visual impairments were recovered in 10 of 12 patients (83.3%) and tinnitus resolved in 10 out of 11 patients (90.9%). In 12 out of 15 cases, the Frisén papilledema grade scores declined to 1 (0–2). The stented IJVs in all 15 patients kept to sufficient blood flows on computed tomographic venography follow-up without stenting-related adverse events.
Conclusions
Non-thrombotic IJV stenosis may be a potential etiology of IIH. Stenting seems to be a promising option to address the issue of intracranial hypertension from the etiological level, particularly after medical treatment failure.
Supporting Information
Filename | Description |
---|---|
ene13512-sup-0001-SupInfo.docxWord document, 47.6 KB | Table S1. 1. Baseline characteristics of patients with isolated non-thrombotic IJV stenosis. 2. Follow-up clinical characteristics of patients with isolated non-thrombotic IJV stenosis. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
References
- 1Ball AK, Clarke CE. Idiopathic intracranial hypertension. Lancet Neurol 2006; 5: 433–442.
- 2Farb RI, Vanek I, Scott JN, et al. Idiopathic intracranial hypertension: the prevalence and morphology of sinovenous stenosis. Neurology 2003; 60: 1418–1424.
- 3Friedman DI, Liu GT, Digre KB. Revised diagnostic criteria for the pseudotumor cerebri syndrome in adults and children. Neurology 2013; 81: 1159–1165.
- 4Frisen L. Swelling of the optic nerve head: a staging scheme. J Neurol Neurosurg Psychiatry 1982; 45: 13–18.
- 5Riggeal BD, Bruce BB, Saindane AM, et al. Clinical course of idiopathic intracranial hypertension with transverse sinus stenosis. Neurology 2013; 80: 289–295.
- 6Higgins JN, Cousins C, Owler BK, Sarkies N, Pickard JD. Idiopathic intracranial hypertension: 12 cases treated by venous sinus stenting. J Neurol Neurosurg Psychiatry 2003; 74: 1662–1666.
- 7Radvany MG, Solomon D, Nijjar S, et al. Visual and neurological outcomes following endovascular stenting for pseudotumor cerebri associated with transverse sinus stenosis. J Neuroophthalmol 2013; 33: 117–122.
- 8Fields JD, Javedani PP, Falardeau J, et al. Dural venous sinus angioplasty and stenting for the treatment of idiopathic intracranial hypertension. J NeuroIntervent Surg 2013; 5: 62–68.
- 9Ahmed RM, Wilkinson M, Parker GD, et al. Transverse sinus stenting for idiopathic intracranial hypertension: a review of 52 patients and of model predictions. AJNR Am J Neuroradiol 2011; 32: 1408–1414.
- 10King JO, Mitchell PJ, Thomson KR, Tress BM. Cerebral venography and manometry in idiopathic intracranial hypertension. Neurology 1995; 45: 2224–2228.
- 11Kosinski M, Bayliss MS, Bjorner JB, et al. A six-item short-form survey for measuring headache impact: the HIT-6. Qual Life Res 2003; 12: 963–974.
- 12Wall M. Idiopathic intracranial hypertension. Neurol Clin 2010; 28: 593–617.
- 13Sinclair AJ, Kuruvath S, Sen D, et al. Is cerebrospinal fluid shunting in idiopathic intracranial hypertension worthwhile? A 10-year review. Cephalalgia 2011; 31: 1627–1633.
- 14Elder BD, Sankey EW, Goodwin CR, et al. Outcomes and experience with lumbopleural shunts in the management of idiopathic intracranial hypertension. World Neurosurg 2015; 84: 314–319.
- 15Hannerz J, Ericson K. The relationship between idiopathic intracranial hypertension and obesity. Headache 2009; 49: 178–184.
- 16Sinclair AJ, Burdon MA, Nightingale PG, et al. Low energy diet and intracranial pressure in women with idiopathic intracranial hypertension: prospective cohort study. BMJ (Clinical Research Ed) 2010; 341: c2701.
- 17Ko MW, Chang SC, Ridha MA, et al. Weight gain and recurrence in idiopathic intracranial hypertension: a case−control study. Neurology 2011; 76: 1564–1567.
- 18Lyon CJ, Law RE, Hsueh WA. Minireview: adiposity, inflammation, and atherogenesis. Endocrinology 2003; 144: 2195–2200.
- 19Dhungana S, Sharrack B, Woodroofe N. Cytokines and chemokines in idiopathic intracranial hypertension. Headache 2009; 49: 282–285.
- 20Raoof N, Sharrack B, Pepper IM, Hickman SJ. The incidence and prevalence of idiopathic intracranial hypertension in Sheffield, UK. Eur J Neurol 2011; 18: 1266–1268.
- 21Mollan SP, Ball AK, Sinclair AJ, et al. Idiopathic intracranial hypertension associated with iron deficiency anaemia: a lesson for management. Eur Neurol 2009; 62: 105–108.
- 22Glueck CJ, Golnik KC, Aregawi D, et al. Changes in weight, papilledema, headache, visual field, and life status in response to diet and metformin in women with idiopathic intracranial hypertension with and without concurrent polycystic ovary syndrome or hyperinsulinemia. Transl Res 2006; 148: 215–222.
- 23Wall M, Kupersmith MJ, Kieburtz KD, et al. The idiopathic intracranial hypertension treatment trial: clinical profile at baseline. JAMA Neurol 2014; 71: 693–701.
- 24Yri HM, Fagerlund B, Forchhammer HB, Jensen RH. Cognitive function in idiopathic intracranial hypertension: a prospective case−control study. BMJ Open 2014; 4: e004376.
- 25Kunte H, Schmidt F, Kronenberg G, et al. Olfactory dysfunction in patients with idiopathic intracranial hypertension. Neurology 2013; 81: 379–382.
- 26Khoo KF, Kunte H. Olfactory dysfunction in patients with idiopathic intracranial hypertension. Neurology 2014; 82: 189.
- 27Perez MA, Bialer OY, Bruce BB, Newman NJ, Biousse V. Primary spontaneous cerebrospinal fluid leaks and idiopathic intracranial hypertension. J Neuroophthalmol 2013; 33: 330–337.
- 28Duke BJ, Ryu RK, Brega KE, Coldwell DM. Traumatic bilateral jugular vein thrombosis: case report and review of the literature. Neurosurgery 1997; 41: 680–683.
- 29Dashti SR, Nakaji P, Hu YC, et al. Styloidogenic jugular venous compression syndrome: diagnosis and treatment: case report. Neurosurgery 2012; 70: E795–E799.
- 30Wilson M, Browne JD, Martin T, Geer C. Case report: atypical presentation of jugular foramen mass. Am J Otolaryngol 2012; 33: 370–374.
- 31Thandra A, Jun B, Chuquilin M. Papilloedema and increased intracranial pressure as a result of unilateral jugular vein thrombosis. Neuro-Ophthalmology (Aeolus Press) 2015; 39: 179–182.
- 32Wall M, McDermott MP, Kieburtz KD, et al. Effect of acetazolamide on visual function in patients with idiopathic intracranial hypertension and mild visual loss: the idiopathic intracranial hypertension treatment trial. JAMA 2014; 311: 1641–1651.
- 33Celebisoy N, Gokcay F, Sirin H, Akyurekli O. Treatment of idiopathic intracranial hypertension: topiramate vs acetazolamide, an open-label study. Acta Neurol Scand 2007; 116: 322–327.
- 34Spitze A, Malik A, Lee AG. Surgical and endovascular interventions in idiopathic intracranial hypertension. Curr Opin Neurol 2014; 27: 69–74.
- 35Fridley J, Foroozan R, Sherman V, Brandt ML, Yoshor D. Bariatric surgery for the treatment of idiopathic intracranial hypertension. J Neurosurg 2011; 114: 34–39.
- 36Ducruet AF, Crowley RW, McDougall CG, Albuquerque FC. Long-term patency of venous sinus stents for idiopathic intracranial hypertension. J NeuroIntervent Surg 2014; 6: 238–242.
- 37Higgins JN, Garnett MR, Pickard JD, Axon PR. An evaluation of styloidectomy as an adjunct or alternative to jugular stenting in idiopathic intracranial hypertension and disturbances of cranial venous outflow. J Neurol Surg B Skull Base 2017; 78: 158–163.