Masson Catherine
Service de Neurologie, Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110 Clichy.
Presse Med. 2005 Jul 2;34(12):869-77. doi: 10.1016/s0755-4982(05)84067-9.
The rapid development of paraparesis or tetraparesis combined with a bilateral sensory deficit that has a clearly defined rostral border and bladder dysfunction are the principal features of acute transverse myelopathy. Acute partial transverse myelopathy is far much more frequent: its symptoms are asymmetric, sometimes unilateral, and sensory deficit may predominate. An urgent MRI is required to exclude acute spinal cord compression. Diagnosis of ischemic acute transverse myelopathy includes the following elements: sudden onset, neurologic symptoms compatible with infarction in the anterior spinal artery area (by far the most frequent location for spinal cord infarction), and presence of a specific cause of spinal cord ischemia. In all other cases where it is difficult to distinguish spinal cord infarction from myelitis, analysis of the cerebrospinal fluid is essential. Most cases of inflammatory acute transverse myelopathy can be linked to a defined cause. Multiple sclerosis is a major cause of partial acute transverse myelopathy. MRI lesions are usually small, located in the lateral or posterior part of the spinal cord. Diagnostic elements include multiple lesions of multifocal demyelination on the cerebral MRI, oligoclonal bands in the cerebrospinal fluid, and the absence of clinical or laboratory abnormalities that suggest systemic disease. Neuromyelitis optica, also known as Devic's disease, has often been considered a variant form of multiple sclerosis. Recent immunologic studies confirm the hypothesis that it is a distinct entity. Infectious transverse acute myelitis is often of viral origin. It may result from direct viral stress but more frequently follows immunologically-mediated indirect stress. This acute parainfectious myelitis, like postvaccinal myelitis, may be considered as a spinal single-focus form of acute disseminated encephalomyelitis (ADEM). It is important to distinguish the latter from an initial episode of multiple sclerosis, because their prognosis and treatment differ.
双下肢轻瘫或四肢轻瘫迅速进展,伴有边界清晰的双侧感觉障碍及膀胱功能障碍,是急性横贯性脊髓炎的主要特征。急性部分横贯性脊髓炎更为常见:其症状不对称,有时为单侧性,感觉障碍可能更为突出。需要紧急进行磁共振成像(MRI)以排除急性脊髓压迫。缺血性急性横贯性脊髓炎的诊断包括以下要点:突然起病、与脊髓前动脉区域梗死相符的神经症状(这是脊髓梗死最常见的部位)以及存在脊髓缺血的特定病因。在所有难以区分脊髓梗死与脊髓炎的其他病例中,脑脊液分析至关重要。大多数炎症性急性横贯性脊髓炎病例可与明确病因相关联。多发性硬化是部分急性横贯性脊髓炎的主要病因。MRI病变通常较小,位于脊髓外侧或后部。诊断要点包括脑部MRI上多灶性脱髓鞘的多个病变、脑脊液中的寡克隆带以及无提示全身性疾病的临床或实验室异常。视神经脊髓炎,也称为德维克病,常被认为是多发性硬化的一种变异形式。最近的免疫学研究证实了它是一种独特疾病的假说。感染性横贯性急性脊髓炎通常由病毒引起。它可能由直接病毒感染导致,但更常见的是免疫介导的间接感染。这种急性感染后脊髓炎,与疫苗接种后脊髓炎一样,可被视为急性播散性脑脊髓炎(ADEM)的脊髓单灶形式。将后者与多发性硬化的初始发作区分开来很重要,因为它们的预后和治疗不同。