Alfredo Pedroza , William Escobar , Santiago Pedroza Gómez , Kemel A. Ghotme
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We included patients with a pressure gradient ≥ 8 mm Hg across the transverse sinus stenosis with a minimum clinical and angiographic follow-up of 18 months.</div></div><div><h3>Results</h3><div>Twenty-four patients were eligible for this study and were classified into four clinical categories and two angiographic types. Twelve patients had a history of migraine with different clinical types for several years. All patients had satisfactory angioplasty with a single stent (Wallstent®) and complete resolution of idiopathic intracranial hypertension syndrome and intolerable tinnitus. Only one patient presented a complication (subdural hematoma) and required surgery. Twenty-two patients had an angiographic control five and ten months after angioplasty, showing a stable stent, with no stenosis, and with patent Labbé vein.</div></div><div><h3>Conclusion</h3><div>This case series reports excellent technical and clinical outcomes in all patients with idiopathic intracranial hypertension syndrome and intolerable pulsatile tinnitus due to transverse sinus stenosis treated with endovascular angioplasty. We propose a clinical and angiographic classification that will contribute to optimizing diagnosis and therapeutic decision-making processes.</div></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"5 1","pages":"Article 100354"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Symptomatic transverse sinus stenosis. 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We included patients with a pressure gradient ≥ 8 mm Hg across the transverse sinus stenosis with a minimum clinical and angiographic follow-up of 18 months.</div></div><div><h3>Results</h3><div>Twenty-four patients were eligible for this study and were classified into four clinical categories and two angiographic types. Twelve patients had a history of migraine with different clinical types for several years. All patients had satisfactory angioplasty with a single stent (Wallstent®) and complete resolution of idiopathic intracranial hypertension syndrome and intolerable tinnitus. Only one patient presented a complication (subdural hematoma) and required surgery. 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引用次数: 0
摘要
背景横窦狭窄是特发性颅内高压综合征和无法忍受的搏动性耳鸣综合征的可治疗原因。然而,它经常被诊断不足,得不到治疗。狭窄水平的支架置入术已成为一种替代疗法。本文介绍了临床和血管造影的分类、手术的技术结果以及临床和血管造影的随访。方法采用血管内成形术治疗特发性颅内高压综合征伴横窦狭窄的难治性搏动性耳鸣。我们纳入了横窦狭窄压力梯度≥8 mm Hg的患者,并进行了至少18个月的临床和血管造影随访。结果24例患者入选,分为4种临床类型和2种血管造影类型。12例患者有多年不同临床类型的偏头痛病史。所有患者均采用单支架(Wallstent®)进行了满意的血管成形术,并完全解决了特发性颅内高压综合征和难以忍受的耳鸣。只有一名患者出现并发症(硬膜下血肿)并需要手术。22例患者在血管成形术后5个月和10个月进行血管造影控制,显示支架稳定,无狭窄,labb静脉通畅。结论本病例系列报告了所有特发性颅内高压综合征合并横窦狭窄引起的难治性搏动性耳鸣患者行血管内成形术治疗的良好技术和临床效果。我们提出一个临床和血管造影分类,将有助于优化诊断和治疗决策过程。
Symptomatic transverse sinus stenosis. Clinical and angiographic classification and endovascular therapy: A case series
Background
Transverse sinus stenosis is a treatable cause of idiopathic intracranial hypertension syndrome and intolerable pulsatile tinnitus syndrome. However, it is often underdiagnosed and left untreated. Stenting at the level of stenosis has emerged as an alternative therapy. This paper presents a clinical and angiographic classification, the technical outcome of the procedure, and the clinical and angiographic follow-up.
Methods
We present a case series of idiopathic intracranial hypertension syndrome and intolerable pulsatile tinnitus due to transverse sinus stenosis treated with endovascular angioplasty. We included patients with a pressure gradient ≥ 8 mm Hg across the transverse sinus stenosis with a minimum clinical and angiographic follow-up of 18 months.
Results
Twenty-four patients were eligible for this study and were classified into four clinical categories and two angiographic types. Twelve patients had a history of migraine with different clinical types for several years. All patients had satisfactory angioplasty with a single stent (Wallstent®) and complete resolution of idiopathic intracranial hypertension syndrome and intolerable tinnitus. Only one patient presented a complication (subdural hematoma) and required surgery. Twenty-two patients had an angiographic control five and ten months after angioplasty, showing a stable stent, with no stenosis, and with patent Labbé vein.
Conclusion
This case series reports excellent technical and clinical outcomes in all patients with idiopathic intracranial hypertension syndrome and intolerable pulsatile tinnitus due to transverse sinus stenosis treated with endovascular angioplasty. We propose a clinical and angiographic classification that will contribute to optimizing diagnosis and therapeutic decision-making processes.