Bakhsh Ali, Elmolla Mohamed, Buxton Neil, Brodbelt Andrew
Department of Neurosurgery, NHS, Liverpool, Merseyside, United Kingdom.
Surg Neurol Int. 2022 May 20;13:205. doi: 10.25259/SNI_1084_2021. eCollection 2022.
We describe a case of long-standing intracranial hypotension caused by an iatrogenic arachnoid diverticulum. This case illustrates two learning points. First, excessive CSF absorption may occur through an acquired arachnoid-epidural venous plexus at a dural defect. Second, a long-standing CSF leak may benefit from definitive surgical repair in the first instance.
A 55-year-old female, with known idiopathic intracranial hypertension, presented with disabling chronic low-pressure symptoms after having a lumboperitoneal shunt removed 5 years previously. MRI scan revealed a Chiari I malformation (CMI) and a small dural interruption at the L3/4 space. CT myelography confirmed the abnormality. Intraoperatively, a dural defect and arachnoid bleb with an overlying attachment of adipose tissue and a vessel were found. Postoperatively, the patient has marked resolution of her headaches and dizziness and is mobilizing independently.
Excessive CSF absorption appears to have occurred through an acquired arachnoid-epidural venous plexus. A high index of suspicion for intracranial hypotension is required in patients with low pressure symptoms and a CMI.
我们描述了一例由医源性蛛网膜憩室引起的长期颅内低压病例。该病例说明了两个要点。第一,脑脊液吸收过多可能通过硬脑膜缺损处后天形成的蛛网膜 - 硬膜外静脉丛发生。第二,长期脑脊液漏可能首先受益于确定性手术修复。
一名55岁女性,已知患有特发性颅内高压,在5年前移除腰大池 - 腹腔分流术后出现致残性慢性低压症状。MRI扫描显示Chiari I畸形(CMI)和L3/4间隙处的小硬脑膜中断。CT脊髓造影证实了该异常。术中发现硬脑膜缺损和蛛网膜泡,其上附着有脂肪组织和血管。术后,患者头痛和头晕明显缓解,可独立活动。
脑脊液吸收过多似乎是通过后天形成的蛛网膜 - 硬膜外静脉丛发生的。对于有低压症状和CMI的患者,需要高度怀疑颅内低压。