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急性和亚急性脊髓病的磁共振成像与临床特征

Magnetic Resonance Imaging and Clinical Features in Acute and Subacute Myelopathies.

作者信息

Weidauer Stefan, Wagner Marlies, Nichtweiß Michael

机构信息

Department of Neurology, Sankt Katharinen Hospital, Teaching Hospital of the Goethe University, Frankfurt, Seckbacher Landstraße 65, 60389, Frankfurt/Main, Germany.

Institute of Neuroradiology, Goethe University, Frankfurt, Germany.

出版信息

Clin Neuroradiol. 2017 Dec;27(4):417-433. doi: 10.1007/s00062-017-0604-x. Epub 2017 Jun 30.

DOI:10.1007/s00062-017-0604-x
PMID:28667382
Abstract

Differential diagnosis of acute and subacute transverse myelopathy includes inflammatory, infectious, vascular, metabolic and paraneoplastic etiologies. Information on the diagnostic approach to transverse myelopathy with regard to daily clinical practice is provided. The differentiation between five lesion patterns on magnetic resonance imaging (MRI) in myelitis may be helpful: (1) longitudinal extensive transverse myelitis, (2) short segment ovoid or peripherally located, (3) "polio-like", (4) granulomatous and (5) segmental with rash. A correlation with these imaging features is supported if the clinical course and neurological symptoms are known. Although the mean interval from onset to nadir of symptoms in spinal cord infarction is 1 h, an overlap with a fulminant course of myelitis is possible, and impaired diffusion may also occur in acute inflammatory processes. As a result, laboratory testing, including aquaporin-4 antibodies and cerebrospinal fluid analysis, is crucial for the correct interpretation of imaging findings. Moreover, the discrimination of acute complete and acute partial transverse myelitis is advantageous in order to identify diverse entities, the latter often being a precursor to multiple sclerosis. Additional brain imaging is mandatory in suspected demyelinating, infectious, neoplastic and systemic autoimmune disease. A symmetrical lesion pattern restricted to individual tracts or dorsal columns indicates subacute combined degeneration of the spinal cord and, in addition to deficiency syndromes, a paraneoplastic etiology should be considered.

摘要

急性和亚急性横贯性脊髓病的鉴别诊断包括炎症性、感染性、血管性、代谢性和副肿瘤性病因。本文提供了关于横贯性脊髓病日常临床诊断方法的信息。脊髓炎磁共振成像(MRI)上五种病变模式的鉴别可能有所帮助:(1)纵向广泛横贯性脊髓炎,(2)短节段卵圆形或位于周边,(3)“脊髓灰质炎样”,(4)肉芽肿性,(5)伴有皮疹的节段性。如果已知临床病程和神经症状,则支持与这些影像学特征相关联。虽然脊髓梗死从发病到症状最低点的平均间隔时间为1小时,但与暴发性脊髓炎病程有重叠的可能,并且在急性炎症过程中也可能出现扩散受限。因此,包括水通道蛋白4抗体和脑脊液分析在内的实验室检查对于正确解读影像学结果至关重要。此外,区分急性完全性和急性部分性横贯性脊髓炎有利于识别不同的疾病实体,后者往往是多发性硬化症的前驱症状。对于疑似脱髓鞘、感染、肿瘤和全身性自身免疫性疾病,必须进行额外的脑部成像检查。局限于个别传导束或后索的对称性病变模式提示脊髓亚急性联合变性,除了缺乏综合征外,还应考虑副肿瘤性病因。

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Toxic and Metabolic Myelopathies.中毒性和代谢性脊髓病
脊髓血管病变:解剖学、成像技术与治疗
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