Shimohata T, Nakano R, Sato S, Tsuji S
Department of Neurology, Niigata University.
Rinsho Shinkeigaku. 1994 Jul;34(7):707-11.
Tapia's syndrome, first described in 1904 by A.G. Tapia, is considered to be a syndrome consisting of ipsilateral hemiplegia of larynx and tongue with spared movement of soft palate. A 61-year-old Japanese woman had been in good health until August 1991, when she developed hoarseness and atrophy of the left side of her tongue. Although she also showed mild disturbance of elevation of bilateral soft palates and loss of taste in the posterior third of her tongue as well, the main symptoms were the paralyses of the ipsilateral larynx and tongue without involvement of the ipsilateral sternocleidomastoid and trapezius muscles. We concluded that she had cranial polyneuropathy similar to that of Tapia's syndrome. A carotid angiography revealed that she has a large aneurysm, which originated from the extracranial internal carotid artery in the region near the skull base. No other abnormal findings were detected by any computed tomography, magnetic resonance imaging or 67Ga-scintigraphy. The patient's lower cranial polyneuropathy was considered to be caused by the aneurysm. A survey of the literature indicates that extracranial carotid aneurysm is an extremely rare cause of Tapia's syndrome. In this case, the location of the aneurysm, which was present considerably distant from the skull base, seems to be the reason for the sparing of the accessory nerve.
塔皮亚综合征由A.G. 塔皮亚于1904年首次描述,被认为是一种由同侧喉和舌偏瘫以及软腭运动保留组成的综合征。一名61岁的日本女性在1991年8月之前一直身体健康,之后出现声音嘶哑和左侧舌萎缩。尽管她还表现出双侧软腭轻度上抬障碍以及舌后三分之一味觉丧失,但主要症状是同侧喉和舌麻痹,同侧胸锁乳突肌和斜方肌未受累。我们得出结论,她患有与塔皮亚综合征类似的颅多神经病。颈动脉血管造影显示她有一个大动脉瘤,起源于颅底附近区域的颅外颈内动脉。计算机断层扫描、磁共振成像或67镓闪烁扫描均未发现其他异常。患者的下颅多神经病被认为是由动脉瘤引起的。文献调查表明,颅外颈动脉瘤是塔皮亚综合征极其罕见的病因。在本病例中,动脉瘤的位置距颅底相当远,这似乎是副神经未受累的原因。