Department of Neurosurgery, Cannizzaro Hospital, Catania, Italy.
Department of Neurosurgery, Azienda Ospedaliera di Rilievo Nazionale e di Alta Specializzazione Garibaldi, Catania, Sicilia, Italy.
J Neurol Surg A Cent Eur Neurosurg. 2023 Mar;84(2):206-211. doi: 10.1055/s-0041-1725049. Epub 2021 Jun 2.
Vertebrobasilar dolichoectasia (VBDE) is defined as a symptomatic dilatation and tortuosity of the vertebrobasilar arteries. The risk of hydrocephalus development is due to direct compression of the third ventricle outflow or brainstem compression and related aqueduct stenosis. We present an uncommon case of a patient with symptomatic VBDE with the uniqueness of a hypoplastic third ventricle associated with biventricular hydrocephalus. A literature review concerning diagnosis and management of patients affected by biventricular hydrocephalus caused by VBDE was also performed.
We report a case of a 54-year-old man who presented with headache, ideomotor apraxia, and gait disorder. A head computed tomography (CT) scan showed a biventricular hydrocephalus and a subsequent CT angiography documented the presence of a VBDE compressing the anterior part of the third ventricle that also appeared hypoplastic. The patient also presented a clinical history of arterial hypertension for which he was given a proper pharmacologic treatment with symptom relief. A surgical treatment of ventriculoperitoneal shunt along with endoscopic septostomy was proposed, but the patient refused, probably due to the slightly positive response to medical treatment.
The natural clinical history of patients affected by VBDE is unfavorable with 7.8 years of median survival. The therapeutic strategy is usually conservative and the role of antiplatelets or oral anticoagulants is still debated. In selected patients, ventriculoperitoneal shunt to resolve intracranial hypertension caused by biventricular hydrocephalus is the most effective treatment. In our opinion, chronic third ventricle compression could lead to anatomic-pathologic alterations like the third ventricle hypoplasia documented in our report.
椎基底动脉延长扩张症(vertebrobasilar dolichoectasia,VBDE)定义为椎基底动脉的症状性扩张和迂曲。脑积水发展的风险是由于第三脑室流出道或脑干受压和相关导水管狭窄直接压迫所致。我们报告了一例伴有第三脑室发育不全的症状性 VBDE 患者,其特征为伴有双侧脑室脑积水。还对因 VBDE 引起的双侧脑室脑积水患者的诊断和治疗进行了文献复习。
我们报告了一例 54 岁男性患者,因头痛、运动性失用症和步态障碍就诊。头部 CT 扫描显示双侧脑室脑积水,随后的 CT 血管造影显示 VBDE 压迫第三脑室前部,第三脑室也显得发育不全。患者还伴有动脉高血压的临床病史,对此他接受了适当的药物治疗,症状缓解。提出了脑室-腹腔分流术联合内镜隔切开术的手术治疗方案,但患者拒绝了,可能是由于对药物治疗有轻微的积极反应。
患有 VBDE 的患者的自然临床病程不利,中位生存期为 7.8 年。治疗策略通常是保守的,抗血小板或口服抗凝剂的作用仍存在争议。在选择的患者中,脑室-腹腔分流术以解决由双侧脑室脑积水引起的颅内高压是最有效的治疗方法。在我们看来,慢性第三脑室受压可导致解剖病理改变,如我们报告中记录的第三脑室发育不全。