Cedzich C, Lunkenheimer A, Baier G, Müller J, Kühner A
Department of Neurosurgery, Breslauer Strasse 201, D-90340 Nürnberg, Germany.
Childs Nerv Syst. 1999 Sep;15(9):472-6. doi: 10.1007/s003810050442.
Since the Dandy-Walker syndrome was first described by Dandy and Blackfan, Taggart and Walker, the many variants of posterior fossa anomalies, the appropriate management of these malformations and the clinical outcome have been the subjects of controversy. Surgery of the posterior fossa with membrane excision was initially the preferred method of treatment. Unfortunately, there was a high rate of complications, and many of the patients treated in this way still needed a shunting system. Ventricular-peritoneal and/or cysto-peritoneal shunting is commonly used to treat symptomatic posterior fossa cysts of Dandy-Walker malformations and hydrocephalus. Cysto-peritoneal shunt implantation only was associated with a high rate of complications, and most patients so treated needed a ventriculo-peritoneal shunt in addition. According to the literature, combined ventriculo-peritoneal and cysto-peritoneal shunting is needed for satisfactory decompression of Dandy-Walker cyst and hydrocephalus in between 16% and 92% of cases. We report on a young patient with a Dandy-Walker malformation who needed drainage of the posterior fossa and a ventricular shunt. We decided to drain the cyst and the supratentorial ventricles via a single, especially prepared, catheter with many perforations. The catheter was inserted under ultrasound guidance. The tube was inserted from the left lateral ventricle through the foramen of Monro into the III ventricle and downwards into the cyst. Intraoperatively, an immediate decrease in the size of the cyst and the supratentorial ventricles was observed. Postoperative MRI confirmed the exact position of the catheter and sufficient drainage of the posterior fossa cyst and the ventricles. Six months later the girl was seen in our outpatient department. Clinical examination showed no neurological deficit, and MRI demonstrated sufficient drainage of the ventricles and the Dandy-Walker malformation, and in addition hypoplasia of the corpus callosum.
自从丹迪-沃克综合征首次由丹迪和布莱克范、塔加特和沃克描述以来,后颅窝畸形的多种变体、这些畸形的恰当处理方法以及临床结果一直是争议的主题。最初,后颅窝膜切除术是首选的治疗方法。不幸的是,并发症发生率很高,许多接受这种治疗的患者仍需要分流系统。脑室-腹腔和/或囊肿-腹腔分流术常用于治疗丹迪-沃克畸形的有症状后颅窝囊肿和脑积水。仅进行囊肿-腹腔分流术植入的并发症发生率很高,大多数接受这种治疗的患者还需要另外进行脑室-腹腔分流术。根据文献,在16%至92%的病例中,需要联合脑室-腹腔和囊肿-腹腔分流术才能使丹迪-沃克囊肿和脑积水得到满意的减压。我们报告了一名患有丹迪-沃克畸形的年轻患者,他需要进行后颅窝引流和脑室分流。我们决定通过一根特别制备的、有许多穿孔的单导管来引流囊肿和幕上脑室。该导管在超声引导下插入。导管从左侧脑室经孟氏孔插入第三脑室,然后向下插入囊肿。术中观察到囊肿和幕上脑室大小立即减小。术后磁共振成像(MRI)证实了导管的准确位置以及后颅窝囊肿和脑室的充分引流。六个月后,这名女孩在我们的门诊部就诊。临床检查未发现神经功能缺损,MRI显示脑室和丹迪-沃克畸形引流充分,此外还发现胼胝体发育不全。