A. V. Zarutskaya, E. V. Mukhina, M. V. Panteleeva, P. K. Zul’ fugarov
{"title":"Differential diagnosis of acute flaccid paralysis in children with Guillain—Barré syndrome and neuromyelitis optica spectrum disorder: Clinical cases","authors":"A. V. Zarutskaya, E. V. Mukhina, M. V. Panteleeva, P. K. Zul’ fugarov","doi":"10.25207/1608-6228-2024-31-1-99-110","DOIUrl":null,"url":null,"abstract":"Background. Acute flaccid paralysis is a clinical syndrome characterized by a sudden onset of weakness in one or more limbs with decreased or absent tendon reflexes in the affected limbs. This condition may be a manifestation of such pathologies as Guillain-Barré syndrome and neuromyelitis optica spectrum disorder. Clinical cases description. We describe two clinical cases of Guillain-Barré syndrome in patient M., 7 years old, and neuromyelitis optica spectrum disorder in patient D., 3 years old. In both children, the main clinical manifestation was acute flaccid paralysis. Patient M. was admitted to the Neurological Department of the Moscow Regional Center for Maternity and Childhood Protection with complaints of sharp pronounced weakness in the limbs, inability to walk. According to the disease history, the patient had an acute respiratory viral infection in October 2022. The conducted neurologic examination revealed decreased muscle tone and muscle strength in all limbs, absence of reflexes from the lower limbs. A liquor test was conducted, which revealed increased protein contents. Electroneuromyography detected a pronounced axonal lesion of all motor fibers in the arms and legs. The formulated diagnosis was “Guillain-Barré syndrome, variant of acute motor axonal neuropathy.” The treatment with plasmapheresis and intravenous immunoglobulins showed positive dynamics. In the second case, patient D. was admitted to the Pediatric Infectious Disease Department of Naro-Fominsk Hospital with similar complaints of sharp weakness in the limbs. Neurological examination showed a diffuse decrease in muscle tone, absence of reflexes from all limbs. Elevated protein contents were determined in the liquor. MRI of the cervical spinal cord showed myelitis of segments C3–C7. Negative antibodies to aquaporin-4 were found. The patient was treated with ceftriaxone, methylprednisolone, and plasmapheresis. Then he was transferred to the Neurological Department of the Moscow Regional Center for Maternity and Childhood Protection, where a repeated MRI of the cervicothoracic spinal cord revealed, in addition to myelitis at the level of C3–C7, a lesion of segments from the level of C2 to the medulla oblongata. The formulated diagnosis was “Neuromyelitis optica spectrum disease, seronegative form. Flaccid tetraparesis.” The continued treatment with prednisolone and intravenous immunoglobulin produced positive effect. Conclusion. The presented clinical cases will help neurologists to improve timely diagnosis and treatment of causes of acute flaccid paralysis in children, thereby reducing possible complications, disability, and mortality.","PeriodicalId":17868,"journal":{"name":"Kuban Scientific Medical Bulletin","volume":"63 20","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kuban Scientific Medical Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25207/1608-6228-2024-31-1-99-110","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background. Acute flaccid paralysis is a clinical syndrome characterized by a sudden onset of weakness in one or more limbs with decreased or absent tendon reflexes in the affected limbs. This condition may be a manifestation of such pathologies as Guillain-Barré syndrome and neuromyelitis optica spectrum disorder. Clinical cases description. We describe two clinical cases of Guillain-Barré syndrome in patient M., 7 years old, and neuromyelitis optica spectrum disorder in patient D., 3 years old. In both children, the main clinical manifestation was acute flaccid paralysis. Patient M. was admitted to the Neurological Department of the Moscow Regional Center for Maternity and Childhood Protection with complaints of sharp pronounced weakness in the limbs, inability to walk. According to the disease history, the patient had an acute respiratory viral infection in October 2022. The conducted neurologic examination revealed decreased muscle tone and muscle strength in all limbs, absence of reflexes from the lower limbs. A liquor test was conducted, which revealed increased protein contents. Electroneuromyography detected a pronounced axonal lesion of all motor fibers in the arms and legs. The formulated diagnosis was “Guillain-Barré syndrome, variant of acute motor axonal neuropathy.” The treatment with plasmapheresis and intravenous immunoglobulins showed positive dynamics. In the second case, patient D. was admitted to the Pediatric Infectious Disease Department of Naro-Fominsk Hospital with similar complaints of sharp weakness in the limbs. Neurological examination showed a diffuse decrease in muscle tone, absence of reflexes from all limbs. Elevated protein contents were determined in the liquor. MRI of the cervical spinal cord showed myelitis of segments C3–C7. Negative antibodies to aquaporin-4 were found. The patient was treated with ceftriaxone, methylprednisolone, and plasmapheresis. Then he was transferred to the Neurological Department of the Moscow Regional Center for Maternity and Childhood Protection, where a repeated MRI of the cervicothoracic spinal cord revealed, in addition to myelitis at the level of C3–C7, a lesion of segments from the level of C2 to the medulla oblongata. The formulated diagnosis was “Neuromyelitis optica spectrum disease, seronegative form. Flaccid tetraparesis.” The continued treatment with prednisolone and intravenous immunoglobulin produced positive effect. Conclusion. The presented clinical cases will help neurologists to improve timely diagnosis and treatment of causes of acute flaccid paralysis in children, thereby reducing possible complications, disability, and mortality.
背景。急性弛缓性麻痹是一种临床综合征,其特点是突然出现一侧或多侧肢体无力,患肢腱反射减弱或消失。这种情况可能是吉兰-巴雷综合征和神经脊髓炎视网膜频谱障碍等病症的一种表现。临床病例描述。我们描述了两个吉兰-巴雷综合征的临床病例,患者 M 患有吉兰-巴雷综合征,7 岁;患者 D 患有神经脊髓炎视网膜频谱障碍,3 岁。这两名儿童的主要临床表现均为急性弛缓性麻痹。患者 M 因四肢无力、无法行走而被送入莫斯科地区妇幼保健中心神经科。病史显示,患者于 2022 年 10 月感染过急性呼吸道病毒。神经系统检查显示四肢肌张力和肌力下降,下肢无反射。进行了酒精测试,结果显示蛋白质含量增加。肌电图检查发现,手臂和腿部的所有运动纤维都有明显的轴索病变。诊断结果为 "格林-巴利综合征,急性运动轴索神经病变"。使用血浆置换术和静脉注射免疫球蛋白的治疗效果良好。在第二个病例中,患者 D 因类似的四肢乏力主诉入住纳罗-福明斯克医院小儿传染病科。神经系统检查显示四肢肌肉张力弥漫性下降,反射消失。在液体中检测到蛋白质含量升高。颈脊髓核磁共振成像显示,C3-C7节段出现脊髓炎。水蒸气素-4抗体呈阴性。患者接受了头孢曲松、甲基强的松龙和血浆置换治疗。随后,他被转到莫斯科地区妇幼保健中心的神经科,在那里对颈胸脊髓进行的磁共振成像检查发现,除了C3-C7水平的脊髓炎外,从C2水平到延髓的脊髓段也出现了病变。诊断结果为 "神经脊髓炎视网膜频谱病,血清阴性。弛缓性四肢瘫痪"。泼尼松龙和静脉注射免疫球蛋白的持续治疗产生了积极效果。结论本临床病例有助于神经科医生及时诊断和治疗儿童急性弛缓性麻痹的病因,从而减少可能出现的并发症、残疾和死亡率。