Rath G P, Bithal P K, Chaturvedi A
Department of Neuroanaesthesiology, Neurosciences Centre, All India Institute of Medical Sciences, New Delhi, India.
Pediatr Neurosurg. 2006;42(6):379-82. doi: 10.1159/000095569.
Myelomeningocele with Chiari II malformation and hydrocephalus is a common association seen in infants with a congenital failure of neurulation. Here we report two cases of such an association presenting with different sets of problems. The first patient presented with severe inspiratory stridor due to bilateral abductor vocal cord paralysis, which was relieved completely within 24 h of definitive surgery. The second patient experienced intraoperative cardiac arrest. Definitive surgery was followed after successful cardiopulmonary resuscitation. The cause of the perioperative sequence of events in both cases is attributed to the associated pathologies of Chiari II malformation.
脊髓脊膜膨出合并Chiari II型畸形和脑积水是先天性神经发育异常婴儿中常见的关联病症。在此,我们报告两例出现不同问题组合的此类关联病例。首例患者因双侧声带外展麻痹出现严重吸气性喘鸣,在确定性手术后24小时内完全缓解。第二例患者术中发生心脏骤停。成功进行心肺复苏后进行了确定性手术。两例患者围手术期一系列事件的原因均归因于Chiari II型畸形的相关病理改变。