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[脊髓空洞症患者的短潜伏期体感诱发电位]

[Short latency somatosensory evoked potentials in patients with syringomyelia].

作者信息

Nagahiro S, Matsukado Y, Wada S, Urasaki E, Fukumura A

出版信息

No To Shinkei. 1986 Nov;38(11):1057-63.

PMID:3814435
Abstract

Short latency somatosensory evoked potentials (SSEPs) following median nerve and posterior tibial nerve stimulation were studied in six patients with syringomyelia. Three patients had Chiari malformations, two patients experienced fracture of the spine and one patient had a cauda equina ependymoma. SSEPs following median nerve stimulation were abnormal in all patients, of which five patients showed abnormal SSEPs only in the unilateral stimulation on the side of sensory deficits. SSEPs obtained from three out of eight upper extremities which showed no disturbance of deep sensation, were abnormal, so SSEPs were able to detect subclinical abnormality indicating dorsal column dysfunction. Abnormal patterns of SSEPs were classified in three types as follows; Type 1: disappearance of P13, N16 and N18 (3 cases), Type 2: the prolonged interpeak latency P11-P13 (2 cases), and Type 3: abnormal N16 and N18 with preserving P13 (1 case with Chiari malformation). P9 and P11 were present without prolonged latencies in all cases. SSEPs following posterior tibial nerve stimulation were abnormal in two of the three tested patients. Those two patients had disturbance of deep sensations in the lower extremities. All patients underwent surgical treatment, syringo-peritoneal shunt in four patients, foramen magnum decompression with syringo-subarachnoid shunt in one patient, and total removal of an ependymoma of the cauda equina with syringotomy in one patient. Postoperative neurological improvement were found in three patients, of which two cases also showed improvement in SSEPs. On the contrary SSEPs were unchanged in two patients with posttraumatic syringomyelia, whose postoperative neurological condition was also unchanged.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对6例脊髓空洞症患者进行了正中神经和胫后神经刺激后的短潜伏期体感诱发电位(SSEPs)研究。3例患者有Chiari畸形,2例患者有脊柱骨折,1例患者有马尾室管膜瘤。所有患者正中神经刺激后的SSEPs均异常,其中5例患者仅在感觉缺失侧的单侧刺激时SSEPs异常。在8例无深部感觉障碍的上肢中,有3例的SSEPs异常,因此SSEPs能够检测出提示背柱功能障碍的亚临床异常。SSEPs的异常模式分为以下三种类型:1型:P13、N16和N18消失(3例);2型:P11 - P13峰间潜伏期延长(2例);3型:P13保留,N16和N18异常(1例Chiari畸形患者)。所有病例中P9和P11均存在且潜伏期未延长。3例接受测试的患者中,2例胫后神经刺激后的SSEPs异常。这2例患者下肢有深部感觉障碍。所有患者均接受了手术治疗,4例行脊髓空洞 - 腹膜分流术,1例行枕骨大孔减压并脊髓空洞 - 蛛网膜下腔分流术,1例行马尾室管膜瘤全切并脊髓空洞切开术。3例患者术后神经功能有改善,其中2例SSEPs也有改善。相反,2例创伤后脊髓空洞症患者的SSEPs未改变,其术后神经状况也未改变。(摘要截断于250字)

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