McGillion Stephen F, Weston-Simons Sam, Harvey Jason R
Department of Orthopaedics, Queen Alexandra Hospital, Portsmouth Hospitals NHS Trust, Cosham, Portsmouth PO6 3LY, UK.
J Spinal Disord Tech. 2009 Aug;22(6):456-8. doi: 10.1097/BSD.0b013e318185d31a.
This study is a case report demonstrating a rare clinical presentation of vertebral artery dissection. We believe that this is the first reported case with multilevel combined sensorimotor radiculopathy. We have also included a literature review.
The purpose of this report is to inform the reader of a unique clinical presentation and to draw attention to some of the rare features of extracranial vertebral artery dissection. We believe that this condition is perhaps underrecognized and this paper may help to increase awareness, thereby encouraging prompt investigation, diagnosis, and implementing early treatment. The literature review also includes a brief anatomic and physiologic description of the underlying pathologic process.
Only a small number of similar cases are described in the literature, though most describe a motor deficit at a single root level. Our case included both motor and sensory deficits at more than 1 level and we describe the possible physiologic and anatomic reasons for this.
The case described is one that presented to our institution and was initially assessed by the first (corresponding) author. The literature review is based on articles identified from a PubMed search on vertebral artery dissection.
The clinical and radiologic findings are discussed in the case report.
Peripheral motor deficits are a rare clinical presentation of spontaneous vertebral artery dissection and tend to affect a solitary root level, typically C5. Sensation is usually preserved. We describe a case presenting with multilevel combined sensorimotor radiculopathy, which we believe has not previously been reported.
本研究为一例报告,展示了椎动脉夹层的罕见临床表现。我们认为这是首例报告的伴有多节段联合感觉运动性神经根病的病例。我们还纳入了文献综述。
本报告的目的是告知读者一种独特的临床表现,并提请注意颅外椎动脉夹层的一些罕见特征。我们认为这种情况可能未得到充分认识,本文可能有助于提高认识,从而鼓励及时进行检查、诊断和实施早期治疗。文献综述还包括对潜在病理过程的简要解剖和生理描述。
文献中仅描述了少数类似病例,尽管大多数病例描述的是单一神经根水平的运动功能缺损。我们的病例包括多个节段的运动和感觉功能缺损,我们描述了其可能的生理和解剖学原因。
所描述的病例是在我们机构就诊的,最初由第一(通讯)作者进行评估。文献综述基于通过PubMed搜索椎动脉夹层相关文章得出。
病例报告中讨论了临床和影像学检查结果。
周围性运动功能缺损是自发性椎动脉夹层的罕见临床表现,往往影响单个神经根水平,通常为C5。感觉通常得以保留。我们描述了一例伴有多节段联合感觉运动性神经根病的病例,我们认为此前未曾有过报道。