Sandberg David I, Navarro Ramon, Blanch Josep, Ragheb John
Department of Neurosurgery, University of Miami Miller School of Medicine and Miami Children's Hospital, Miami, Florida 33155, USA.
J Neurosurg. 2007 Jun;106(6 Suppl):490-4. doi: 10.3171/ped.2007.106.6.490.
The authors report on two children in whom an anomalous posterior fossa venous drainage pattern prevented safe posterior fossa decompression. Both patients had Chiari malformation Type I, multisutural craniosynostosis, and crowded posterior fossa structures. Both patients had been treated with ventriculoperitoneal shunts for hydrocephalus. Pfeiffer syndrome had been diagnosed in one of the patients, and the other was suspected to have osteogenesis imperfecta. Although both patients were believed to have symptoms resulting from brainstem compression, posterior fossa decompression was not offered due to profound venous anomalies noted on imaging studies that greatly increased the expected risks associated with surgery. These cases are presented to alert neurosurgeons to carefully evaluate the posterior fossa venous anatomy prior to considering posterior fossa decompression with or without occipitocervical fusion or calvarial vault remodeling procedures in patients with multisutural craniosynostosis.
作者报告了两名儿童,其异常的后颅窝静脉引流模式阻碍了安全的后颅窝减压。两名患者均患有I型Chiari畸形、多缝颅缝早闭和后颅窝结构拥挤。两名患者均因脑积水接受了脑室腹腔分流术治疗。其中一名患者被诊断为Pfeiffer综合征,另一名患者疑似患有成骨不全症。尽管两名患者均被认为有脑干受压导致的症状,但由于影像学研究发现的严重静脉异常大大增加了手术预期风险,因此未进行后颅窝减压。呈现这些病例是为了提醒神经外科医生,在考虑对患有多缝颅缝早闭的患者进行后颅窝减压(无论有无枕颈融合或颅盖重塑手术)之前,要仔细评估后颅窝静脉解剖结构。