Willis J, Van den Bergh P
Department of Pediatrics, Tufts University School of Medicine, Boston, MA.
J Child Neurol. 1988 Jul;3(3):200-4. doi: 10.1177/088307388800300310.
We present two children with seizures and other signs of cerebral involvement at the outset of acute inflammatory demyelinating polyneuropathy, consistent with a diagnosis of encephalomyeloradiculoneuropathy. One child had a recurrence associated with mild central dysfunction and improved during therapy with corticosteroids. Both children recovered completely. Both acute and relapsing inflammatory demyelinating neuropathy may be accompanied by cerebral dysfunction, expanding the clinical spectrum of encephalomyeloradiculoneuropathy.
我们报告了两名儿童,在急性炎症性脱髓鞘性多发性神经病起病时出现癫痫发作及其他脑受累迹象,符合脑脊髓神经根神经病的诊断。一名儿童复发时伴有轻度中枢功能障碍,在接受皮质类固醇治疗期间病情好转。两名儿童均完全康复。急性和复发性炎症性脱髓鞘性神经病都可能伴有脑功能障碍,从而扩大了脑脊髓神经根神经病的临床谱。