Emiroglu Melike, Alkan Gulsum, Kartal Ayse, Cimen Derya
Department of Pediatric Infectious Diseases, Selcuk University Faculty of Medicine, Alaeddin Keykubat Campus, 42075, Selcuklu, Konya, Turkey.
Department of Pediatric Neurology, Selcuk University Faculty of Medicine, Konya, Turkey.
Rheumatol Int. 2016 Aug;36(8):1181-3. doi: 10.1007/s00296-016-3515-2. Epub 2016 Jun 21.
Kawasaki disease (KD) is a systemic vasculitis that can involve the nervous system, including the cranial nerves. Central nervous system findings, especially irritability, lethargy, and aseptic meningitis, occur in 1-30 % of KD patients (1). Cranial nerve palsies are seen rarely, and abducens nerve palsy has been reported in only three children. We describe a 2.5-year-old girl with incomplete KD who developed transient abducens nerve palsy after intravenous immunoglobulin (IVIG) treatment.
川崎病（KD）是一种全身性血管炎，可累及神经系统，包括颅神经。中枢神经系统表现，尤其是易激惹、嗜睡和无菌性脑膜炎，见于1%-30%的KD患者（1）。颅神经麻痹很少见，仅报道过3例儿童发生外展神经麻痹。我们描述了一名2.5岁患不完全性KD的女孩，在静脉注射免疫球蛋白（IVIG）治疗后出现了短暂性外展神经麻痹。
