Aoki N
Department of Neurosurgery, Tokyo Metropolitan Fuchu Hospital, Japan.
Surg Neurol. 1988 Aug;30(2):153-5. doi: 10.1016/0090-3019(88)90103-6.
A sudden onset of quadriplegia and dyspnea occurred in a 4-year-old girl with Down's syndrome, who had been noted to have atlantoaxial dislocation. She underwent cervical immobilization initially with a halo-vest and subsequently by posterior fusion, resulting in significant functional recovery. The catastrophic myelopathy that occurred in this patient emphasizes the necessity of treatment even for asymptomatic atlantoaxial instability in some individuals with Down's syndrome.
一名患有唐氏综合征的4岁女孩突然出现四肢瘫痪和呼吸困难,此前已发现她存在寰枢椎脱位。她最初通过头环背心进行颈部固定,随后接受了后路融合术,功能得到了显著恢复。该患者发生的灾难性脊髓病强调,对于一些唐氏综合征患者即使是无症状的寰枢椎不稳也有治疗的必要性。