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Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report

机译:肠道病毒D68引起的支气管哮喘首发后的霍普金斯综合征:一例报告

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Hopkins syndrome (HS) is a rare disorder presenting with acute flaccid paralysis of the limbs following an asthma attack. Neurologists encounter a diagnostic challenge if patients without a history of bronchial asthma develop neurologic features mimicking HS following acute respiratory distress. We report a case of HS occurring after a first episode of bronchial asthma associated with enterovirus D68 infection. A 5-year-old girl developed acute respiratory distress. On the fourth hospital day, both her legs became paralyzed except for slight muscle contraction in the right lower limb. Tendon reflexes in the lower limbs were diminished and there was a positive Babinski sign on the right. Sensation was normal in all modalities, and there was no uro-rectal disturbance. Spinal magnetic resonance imaging identified T2-hyperintense lesions with spinal cord edema, mainly involving the bilateral T11 to L1 anterior horns, with left side dominance extending to the left posterior horn. The neurological and neuro-radiological findings of our case were suggestive of HS; however, she had no history of bronchial asthma. An acetylcholine inhalation challenge eventually proved the presence of reversible airway hyper-responsiveness, allowing us to diagnose HS. We identified enterovirus D68 in the patient’s intratracheal aspirates using a sensitive polymerase chain reaction assay. Intravenous immunoglobulin administrations at 2?g/kg2 for 5 consecutive days were repeated every month up to four times. After these treatments, the muscle strength of her right lower limb slightly improved while her left lower leg remained completely paralyzed. This case emphasizes the importance of provocation tests to reveal the presence of airway hyper-responsiveness when a child shows neurological signs mimicking HS following acute respiratory distress. Furthermore, the present case suggests a possible link between HS and acute flaccid paralysis following lower respiratory tract infection by enterovirus D68.
机译:霍普金斯综合征(HS)是一种罕见的疾病,在哮喘发作后会出现四肢急性弛缓性麻痹。如果没有支气管哮喘病史的患者在急性呼吸窘迫后出现模仿HS的神经系统特征,神经科医生将面临诊断挑战。我们报告一例与肠病毒D68感染相关的支气管哮喘发作后发生HS的病例。一名5岁女孩发展为急性呼吸窘迫。在医院的第四天,除了右下肢的轻微肌肉收缩外,她的双腿都瘫痪了。下肢的肌腱反射减弱,右侧出现Babinski阳性征兆。在所有方式中感觉都是正常的,并且没有尿道直肠疾病。脊柱磁共振成像发现T2高强度病变伴脊髓水肿,主要累及双侧T11至L1前角,左侧优势延伸至左后角。本病例的神经和神经放射学结果提示HS。但是,她没有支气管哮喘病史。吸入乙酰胆碱的挑战最终证明了可逆性气道高反应性的存在,使我们能够诊断HS。我们使用敏感的聚合酶链反应分析法在患者气管内抽吸物中鉴定出肠道病毒D68。每月连续2天以2?g / kg2的剂量连续静脉注射免疫球蛋白,最多重复4次。经过这些治疗后,她的右下肢的肌肉力量略有改善,而她的左小腿仍然完全瘫痪。这个案例强调了激发试验的重要性,当孩子表现出模仿急性呼吸窘迫的HS的神经系统体征时,激发试验才能揭示气道高反应性的存在。此外,本病例表明,肠道病毒D68感染下呼吸道后,HS与急性弛缓性麻痹之间可能存在联系。

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