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Pathogenesis of syringomyelia associated with Chiari type 1 malformation: review of evidences and proposal of a new hypothesis.与 Chiari Ⅰ 型畸形相关的脊髓空洞症的发病机制:证据回顾与新假说的提出。
Neurosurg Rev. 2010 Jul;33(3):271-84; discussion 284-5. doi: 10.1007/s10143-010-0266-5. Epub 2010 Jun 8.
3
Syringomyelia with quadriparesis in CSF shunt malfunction: a case illustration.脑脊液分流功能障碍伴四肢瘫痪的脊髓空洞症:病例说明
Childs Nerv Syst. 2010 Sep;26(9):1229-31. doi: 10.1007/s00381-010-1165-3. Epub 2010 May 6.
4
Terminal syringomyelia mimicking an intramedullary tumor: case report.酷似髓内肿瘤的终末期脊髓空洞症:病例报告
Turk Neurosurg. 2010 Apr;20(2):247-50. doi: 10.5137/1019-5149.JTN.1736-09.1.
5
Malformations of the craniocervical junction (Chiari type I and syringomyelia: classification, diagnosis and treatment).颅颈交界区畸形(Chiari Ⅰ型和脊髓空洞症:分类、诊断和治疗)。
BMC Musculoskelet Disord. 2009 Dec 17;10 Suppl 1(Suppl 1):S1. doi: 10.1186/1471-2474-10-S1-S1.
6
Syringomyelia with syringobulbia presenting as vocal fold paralysis.表现为声带麻痹的脊髓空洞症合并延髓空洞症
Ear Nose Throat J. 2009 Jul;88(7):E20.
7
Spinal arteriovenous malformation associated with syringomyelia.脊髓动静脉畸形伴脊髓空洞症。
J Neurosurg Spine. 2009 May;10(5):436-42. doi: 10.3171/2009.2.SPINE08172.
8
Unraveling the riddle of syringomyelia.揭开脊髓空洞症之谜。
Neurosurg Rev. 2006 Oct;29(4):251-63; discussion 264. doi: 10.1007/s10143-006-0029-5. Epub 2006 May 31.
9
Gowers intrasyringal hemorrhage. Case report and review of the literature.高尔斯氏脊髓空洞内出血。病例报告及文献综述。
J Neurosurg Spine. 2005 Dec;3(6):477-81. doi: 10.3171/spi.2005.3.6.0477.
10
Paraparesis secondary to expansion of cervical syrinx: an unusual presentation of ventriculo-peritoneal shunt malfunction.颈髓空洞症扩张继发的双下肢轻瘫:脑室-腹腔分流术故障的一种罕见表现。
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1型Arnold-Chiari畸形合并脊髓空洞症表现为急性四肢轻瘫:一例报告

Arnold-Chiari 1 malformation type 1 with syringohydromyelia presenting as acute tetraparesis: a case report.

作者信息

Schneider Byron, Birthi Pravardhan, Salles Sara

机构信息

University of Kentucky, Lexington, KY, USA.

出版信息

J Spinal Cord Med. 2013 Mar;36(2):161-5. doi: 10.1179/2045772312Y.0000000047.

DOI:10.1179/2045772312Y.0000000047
PMID:23809533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3595966/
Abstract

CONTEXT

A 19-year-old woman who presented to a community hospital after awakening with tetraparesis, generalized paresthesia, and severe neck pain, and was transferred to an acute care hospital.

FINDINGS

Magnetic resonance imaging of the head and spine was performed and revealed a cystic lesion extending from the C1 level to the C6 level as well as an Arnold-Chiari type 1 malformation. Emergent surgical posterior fossa decompression with duraplasty and C1 laminectomy was undertaken. Most symptoms improved immediately postoperatively. On post-operative day 15, the patient was transferred to our acute rehabilitation hospital for an additional 16 days. With continued aggressive therapy, she demonstrated complete resolution of tetraparesis as well as significant improvement in muscle strength and function in addition to resolution of paresthesia and neck pain. Functional independence measure scores were 69/126 on admission to 110/126 on discharge from the rehabilitation hospital. Her tetraparesis eventually resolved; manual muscle testing scores on follow-up 2 months later were 5/5 in all four extremities.

CLINICAL RELEVANCE

This is the first reported case of Chiari I malformation with syringohydromyelia presenting as acute tetraparesis, generalized paresthesia, and neck pain. Surgical decompression leading to resolution of symptoms made other etiologies extremely unlikely and there was no history of trauma. The different theories on the pathogenesis of syringomyelia are discussed.

摘要

背景

一名19岁女性在醒来后出现四肢瘫痪、全身感觉异常和严重颈部疼痛,先到社区医院就诊,后被转至一家急症医院。

检查结果

对头部和脊柱进行了磁共振成像检查,发现一个囊性病变从C1水平延伸至C6水平,以及1型阿诺德-基亚里畸形。紧急进行了后颅窝减压术并硬脑膜成形术以及C1椎板切除术。术后大多数症状立即得到改善。术后第15天,患者被转至我们的急性康复医院,又接受了16天的治疗。通过持续积极治疗,她的四肢瘫痪完全消失,肌肉力量和功能显著改善,感觉异常和颈部疼痛也消失了。功能独立性测量评分从入院时的69/126提高到康复医院出院时的110/126。她的四肢瘫痪最终得以解决;2个月后的随访中,所有四肢的徒手肌力测试评分均为5/5。

临床意义

这是首例报告的以急性四肢瘫痪、全身感觉异常和颈部疼痛为表现的伴有脊髓空洞症的1型基亚里畸形病例。手术减压使症状得到缓解,排除了其他病因,且患者没有外伤史。文中讨论了关于脊髓空洞症发病机制的不同理论。