Moon Ju-Sun, Il Kim Gwang, Koo Young-Ho, Kim Hyun-Sook, Kim Won-Chan, Kim Ok-Joon, Oh Seung-Hun
Department of Neurology, Pochon CHA University college of medicine, South Korea.
J Neurol Sci. 2009 Feb 15;277(1-2):181-3. doi: 10.1016/j.jns.2008.10.021. Epub 2008 Nov 22.
Involvement of central nervous system occasionally occurs as a form of aseptic meningitis in Kikuchi-Fujimoto disease (KFD). However, acute cerebellar symptoms are very rare in KFD. We describe a 42 year-old woman presenting kinetic tremor and gait ataxia preceding cervical lymphadenopathy. The diagnosis of KFD was made based on pathology. Lymphocyte-dominant pleocytosis was observed in cerebrospinal fluid. Brain and spinal magnetic resonance imaging showed no structural abnormalities. Acute cerebellar symptoms and cervical lymphadenopathy disappeared spontaneously within 2 months. This case of KFD involved unusual acute cerebellar symptoms. Selective involvement of the cerebellar system by viral or immunologic response may be attributed to acute cerebellar symptoms in KFD.
中枢神经系统受累在菊池-藤本病(KFD)中偶尔以无菌性脑膜炎的形式出现。然而,KFD中急性小脑症状非常罕见。我们描述了一名42岁女性,在颈部淋巴结病之前出现运动性震颤和步态共济失调。KFD的诊断基于病理学。脑脊液中观察到以淋巴细胞为主的细胞增多。脑和脊髓磁共振成像未显示结构异常。急性小脑症状和颈部淋巴结病在2个月内自发消失。该例KFD伴有不寻常的急性小脑症状。病毒或免疫反应对小脑系统的选择性累及可能是KFD中急性小脑症状的原因。