Tali E Turgut, Ercan Nil, Kaymaz Memduh, Pasaoglu Aydin, Jinkins J Randy
Department of Radiology, Division of Neuroradiology, Gazi University School of Medicine, 06510 Ankara, Turkey.
Neuroradiology. 2004 Sep;46(9):744-54. doi: 10.1007/s00234-004-1240-0.
This study was designed to assess the feasibility of intrathecal gadolinium-enhanced magnetic resonance cisternography (MRC) for the evaluation of the presence or absence of communication of cranial arachnoid cysts with the cerebrospinal fluid (CSF) pathways of the central nervous system (CNS). This prospective study included 20 patients (12 males and 8 females) with a mean age of 37 years, who had, as a group, 22 intracranial arachnoid cysts identified on prior CT and/or MR examinations. Routine pre-contrast cranial MR imaging was followed by the intrathecal administration of 0.5 cc gadopentetate dimeglumine (GD) (Magnevist, Schering, Germany). Immediate and delayed (24 h) MR cisternography was then carried out. Eleven of 22 arachnoid cysts showed immediate CSF communication by the demonstration GD-contrast enhancement of the cyst fluid on the immediate post-injection scan. Contrast enhancement of the cyst was observed only on delayed MRC in six patients. MR imaging in five patients demonstrated no contrast enhancement of the arachnoid cysts on either immediate or delayed imaging. Six patients had mild transient post-procedure headache that was relieved by oral analgesics within 24 h. No serious immediate or chronic adverse effects or complications relating to the intrathecal contrast administration were observed. This study showed the relative safety, feasibility and reliability of low-dose intrathecal GD MR imaging in the demonstration of the communication or non-communication of intracranial arachnoid cysts with the CSF pathways of the CNS. In the future, this may have bearing on the selection for surgery of patients with intracranial arachnoid cysts presenting with clinical signs and symptoms potentially related to the location and mass effect of the cyst.
本研究旨在评估鞘内注射钆增强磁共振脑池造影(MRC)用于评估颅内蛛网膜囊肿与中枢神经系统(CNS)脑脊液(CSF)通路是否相通的可行性。这项前瞻性研究纳入了20例患者(12例男性和8例女性),平均年龄37岁,这些患者在之前的CT和/或MR检查中总共发现了22个颅内蛛网膜囊肿。在进行常规的对比剂前头颅MR成像后,鞘内注射0.5 cc钆喷酸葡胺(GD)(马根维显,德国先灵公司)。然后立即及延迟(24小时)进行磁共振脑池造影。22个蛛网膜囊肿中有11个在注射后立即扫描时显示囊肿液有GD对比剂增强,提示立即与脑脊液相通。6例患者仅在延迟MRC时观察到囊肿有对比剂增强。5例患者的MR成像显示在立即或延迟成像时蛛网膜囊肿均无对比剂增强。6例患者术后出现轻度短暂头痛,24小时内口服镇痛药后缓解。未观察到与鞘内注射对比剂相关的严重即时或慢性不良反应或并发症。本研究表明低剂量鞘内注射GD MR成像在显示颅内蛛网膜囊肿与CNS脑脊液通路相通或不相通方面具有相对安全性、可行性和可靠性。未来,这可能对出现可能与囊肿位置和占位效应相关临床体征和症状的颅内蛛网膜囊肿患者的手术选择有影响。