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Clinical Approach to Pediatric Transverse Myelitis Neuromyelitis Optica Spectrum Disorder and Acute Flaccid Myelitis

机译:小儿横贯性脊髓炎视神经脊髓炎频谱松弛症和急性弛缓性脊髓炎的临床方法

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摘要

Pediatric transverse myelitis (TM) is an acquired, immune-mediated disorder that leads to injury of the spinal cord and often manifests as weakness, numbness, bowel dysfunction, and/or bladder dysfunction. Multiple etiologies for myelitis can result in a similar clinical presentation, including idiopathic transverse myelitis (TM), multiple sclerosis (MS), neuromyeltis optica spectrum disorder (NMOSD) associated with anti-aquaporin 4 antibodies, MOG antibody-associated disease, and acute flaccid myelitis (AFM). Diagnosis relies on clinical recognition of the syndrome and confirming inflammation through imaging and/or laboratory studies. Acute treatment is targeted at decreasing immune-mediated injury, and chronic preventative therapy may be indicated if TM is determined to be a manifestation of a relapsing disorder (i.e., NMOSD). Timely recognition and treatment of acute transverse myelitis is essential, as it can be associated with significant morbidity and long-term disability.
机译:小儿横纹肌炎(TM)是一种获得性的,免疫介导的疾病,可导致脊髓损伤,并通常表现为无力,麻木,肠功能障碍和/或膀胱功能障碍。脊髓炎的多种病因可导致相似的临床表现,包括特发性横贯性脊髓炎(TM),多发性硬化症(MS),与抗水通道蛋白4抗体相关的视神经脊髓炎频谱疾病(NMOSD),与MOG抗体相关的疾病以及急性弛缓脊髓炎(AFM)。诊断依赖于对综合征的临床识别并通过成像和/或实验室研究确认炎症。急性治疗的目标是减少免疫介导的损伤,如果TM被确定为复发性疾病(即NMOSD)的表现,则可能需要进行慢性预防治疗。及时识别和治疗急性横贯性脊髓炎至关重要,因为它可能与明显的发病率和长期残疾相关。

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