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急性弛缓性脊髓炎:临床综述。

Acute Flaccid Myelitis: A Clinical Review.

机构信息

Johns Hopkins Myelitis and Myelopathy Center, Division of Neuroimmunology and Neurological Infections, Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

Semin Neurol. 2020 Apr;40(2):211-218. doi: 10.1055/s-0040-1705123. Epub 2020 Mar 6.

Abstract

Acute flaccid myelitis (AFM) is an emerging disorder primarily affecting children that is characterized by acute flaccid paralysis accompanied by abnormalities of the spinal cord gray matter on magnetic resonance imaging. In most cases, prodromal fever or respiratory symptoms occur, followed by acute-onset flaccid limb weakness. Respiratory, axial, bulbar, facial, and extraocular muscles may also be affected. The clinical manifestations have been described as "polio-like," due to striking similarities to cases of poliomyelitis. The primary site of injury in AFM is the anterior horn cells of the spinal cord, resulting in a motor neuronopathy. Seasonal peaks of cases have occurred in the United States every 2 years since 2012. However, AFM remains a rare disease, which can make it challenging for physicians to recognize and differentiate from other causes of acute flaccid paralysis such as Guillain-Barre syndrome, spinal cord stroke, and transverse myelitis. Epidemiological evidence suggests that AFM is linked to a viral etiology, with nonpolio enteroviruses (in particular enterovirus D68) demonstrating a plausible association. The epidemiology, possible etiological factors, clinical features, differential diagnosis, treatment, and outcomes of AFM are discussed in this review.

摘要

急性弛缓性脊髓炎(AFM)是一种主要影响儿童的新兴疾病,其特征是急性弛缓性瘫痪,伴有磁共振成像上脊髓灰质异常。大多数情况下,会出现前驱发热或呼吸道症状,随后出现急性弛缓性肢体无力。呼吸肌、轴性肌、延髓肌、面肌和眼外肌也可能受到影响。由于与脊髓灰质炎病例惊人地相似,其临床表现被描述为“类脊髓灰质炎”。AFM 的主要损伤部位是脊髓前角细胞,导致运动神经元病。自 2012 年以来,美国每 2 年就会出现一次病例的季节性高峰。然而,AFM 仍然是一种罕见疾病,这使得医生难以识别和区分其与其他急性弛缓性瘫痪的病因,如吉兰-巴雷综合征、脊髓卒中、横贯性脊髓炎等。流行病学证据表明,AFM 与病毒病因有关,非脊髓灰质炎肠道病毒(特别是肠道病毒 D68)显示出合理的相关性。本文综述了 AFM 的流行病学、可能的病因因素、临床特征、鉴别诊断、治疗和预后。

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