Nakamura Yoshikazu, Ikeda Ken, Yoshii Yasuhiro, Ito Hirono, Hirayama Takehisa, Kawabe Kiyokazu, Kano Osamu, Iwasaki Yasuo
Department of Neurology, Toho University Omori Medical Centre, Japan.
Intern Med. 2011;50(15):1605-9. doi: 10.2169/internalmedicine.50.5027. Epub 2011 Aug 1.
Neuromyelitis optica (NMO) is an inflammatory demyelinating disorder characterized by optic neuritis and acute myelitis. A parainfectious pathogenesis may play a partial role in the development of this disorder. Several viral infections are known to cause NMO. Here we report the case of a 15-year-old girl diagnosed with postinfluenza monophasic NMO. The patient developed sudden fever and chills, and the rapid diagnostic test for influenza was positive. She was diagnosed as influenza A and was treated with zanamivir hydrate (10 mg/day, inhalation). Three days later, she complained of dysuria and dysesthesia in the lower extremities. After nine days, she experienced blurred vision bilaterally. Neurological examination revealed visual disturbance, dysuria, dysesthesia and hyperreflexia in the lower extremities. Her visual acuity was counting fingers in OD and 2/100 in OS. Pupillary size was 4.0 mm and light reflexes were sluggish on both sides. Ophthalmoscopy showed marked edema of the optic discs. Serum influenza immunoglobulin M antibodies were elevated and serum anti-aquaporin 4 (AQP4) antibodies were undetectable. Spinal cord magnetic resonance imaging (MRI) displayed longitudinally extensive lesions in the thoracic cord. Brain MRI disclosed three subcortical lesions. The patient fulfilled the revised diagnostic criteria for NMO (2006). After methylprednisolone pulse therapy followed by oral administration of prednisolone, visual dysfunction, dysuria, limb dysesthesia and hyperreflexia were improved. Subsequently, she experienced no attacks for 3 years. This is the first case report of influenza A-associated NMO with such features of postinfectious NMO as a pediatric onset, monophasic course and anti-AQP4 antibody-seronegative status.
视神经脊髓炎(NMO)是一种以视神经炎和急性脊髓炎为特征的炎性脱髓鞘疾病。感染后发病机制可能在该疾病的发生发展中起部分作用。已知几种病毒感染可导致NMO。在此,我们报告一例15岁女孩诊断为流感后单相NMO的病例。患者突然出现发热和寒战,流感快速诊断检测呈阳性。她被诊断为甲型流感,并接受了扎那米韦水合物(10毫克/天,吸入)治疗。三天后,她诉说排尿困难和下肢感觉异常。九天后,她双侧出现视力模糊。神经系统检查发现视力障碍、排尿困难、感觉异常和下肢反射亢进。她的右眼视力为眼前指数,左眼视力为2/100。双侧瞳孔大小为4.0毫米,光反射迟钝。眼底镜检查显示视盘明显水肿。血清流感免疫球蛋白M抗体升高,血清抗水通道蛋白4(AQP4)抗体未检测到。脊髓磁共振成像(MRI)显示胸段脊髓有纵向广泛病变。脑部MRI显示三个皮质下病变。该患者符合NMO修订诊断标准(2006年)。在甲泼尼龙冲击治疗后口服泼尼松龙,视力障碍、排尿困难、肢体感觉异常和反射亢进得到改善。随后,她3年未发作。这是首例具有小儿发病、单相病程和抗AQP4抗体血清阴性等感染后NMO特征的甲型流感相关NMO病例报告。