Yasuhara Takao, Fukuhara Toru, Nakagawa Minoru, Terai Yoshinori, Yoshino Kimihiro, Mizobuchi Koichi, Fujimoto Shunichiro
Department of Neurosurgery, Kagawa Rosai Hospital, Marugame City, Kagawa, Japan.
J Neurosurg. 2002 Nov;97(5):1229-32. doi: 10.3171/jns.2002.97.5.1229.
The authors describe a unique presentation of Wegener granulomatosis (WG) manifesting predominantly as meningitis. Magnetic resonance imaging demonstrated diffuse meningeal enhancement, including the pia mater, in a 28-year-old man with meningitis. A diagnosis of atypical WG was based on the findings of a dural biopsy sample and an elevated cytoplasmic antineutrophil cytoplasmic antibody (cANCA) titer, although the patient did not have any of the lesions common to WG. Immunosuppressive therapy was quite effective. With treatment, the meningeal enhancement resolved and the cANCA titer normalized. Meningeal granulomatosis as the sole lesion in WG has never been reported in the literature. This atypical course of WG should be noted.
作者描述了以脑膜炎为主的韦格纳肉芽肿(WG)的一种独特表现形式。磁共振成像显示,一名患有脑膜炎的28岁男性存在包括软脑膜在内的弥漫性脑膜强化。尽管该患者没有WG常见的任何病变,但基于硬脑膜活检样本的结果和胞浆抗中性粒细胞胞浆抗体(cANCA)滴度升高,诊断为非典型WG。免疫抑制治疗非常有效。经治疗,脑膜强化消失,cANCA滴度恢复正常。文献中从未报道过脑膜肉芽肿作为WG唯一病变的情况。应注意WG的这种非典型病程。