Okanishi Tohru, Saito Yoshiaki, Miki Shiho, Nagaishi Jun-Ichi, Hanaki Keiichi, Tomita Yutaka, Fukuda Chisako, Fujii Shinya, Fujiwara Kazunori, Kawamoto Katsuyuki, Hata Fumiko, Maegaki Yoshihiro, Ohno Kousaku
Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University, 36-1 Nishi-cho, Yonogo 683-8504, Japan.
Brain Dev. 2007 Apr;29(3):189-92. doi: 10.1016/j.braindev.2006.08.008. Epub 2006 Sep 27.
A 6-month-old boy with persistent primitive trigeminal artery (PPTA) presented with stridor, dysphagia, delayed motor development and postural neck and shoulder dystonia. Magnetic resonance imaging/angiography and ultrasonography revealed PPTA, with flow from the dilated basilar artery to the right internal carotid artery, lower brainstem compression by the dilated basilar artery, and cerebellar vermis hypoplasia. Evoked potentials showed lower pons and medulla oblongata functional disruption. These lesions may be related to vascular etiology in the lower brainstem or to congenital malformation syndrome involving infratentorial structures. The relationship of this condition to Möbius syndrome is discussed.
一名患有持续性原始三叉动脉(PPTA)的6个月大男孩出现喘鸣、吞咽困难、运动发育迟缓以及姿势性颈部和肩部肌张力障碍。磁共振成像/血管造影和超声检查显示存在PPTA,有血流从扩张的基底动脉流向右侧颈内动脉,扩张的基底动脉压迫下脑干,以及小脑蚓部发育不全。诱发电位显示脑桥下部和延髓功能中断。这些病变可能与下脑干的血管病因或涉及幕下结构的先天性畸形综合征有关。本文讨论了这种情况与莫比乌斯综合征的关系。