Snyder W E, Luerssen T G, Boaz J C, Kalsbeck J E
Pediatric Neurosurgery Section, James Whitcomb Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Ind., 46202, USA.
Pediatr Neurosurg. 1998 Sep;29(3):117-20. doi: 10.1159/000028704.
Chiari III malformations are extremely rare hindbrain malformations that are associated with a high early mortality rate, or severe neurologic deficits in the survivors. The preferred treatment is early operative closure and CSF shunting. We report a case of a newborn infant with a Chiari III malformation with displacement of the brainstem and cerebellum into the cervical encephalocele which precluded immediate operative closure of the defect. Instead, a ventriculoperitoneal shunt was placed and the patient was followed with serial imaging studies. The child survived. The shunt allowed the brainstem and cerebellum to regress into the cervical spinal canal as the dilated cerebral aqueduct and fourth ventricle decompressed. A delayed closure of the cervical encephalocele was performed at 30 months of age. Cerebrospinal fluid diversion with delayed closure may be an option for large lesions.
Chiari III型畸形是极其罕见的后脑畸形,与早期高死亡率或幸存者严重神经功能缺损相关。首选治疗方法是早期手术闭合和脑脊液分流。我们报告一例患有Chiari III型畸形的新生儿病例,其脑干和小脑移位至颈脑膨出内,这使得无法立即对缺损进行手术闭合。取而代之的是,放置了脑室腹腔分流管,并通过系列影像学检查对患者进行随访。患儿存活下来。随着扩张的中脑导水管和第四脑室减压,分流管使脑干和小脑退回至颈椎管内。在患儿30个月大时对颈脑膨出进行了延迟闭合。对于大的病变,脑脊液分流并延迟闭合可能是一种选择。