Holzer Katrin, Esposito Lorena, Stimmer Herbert, Hemmer Bernhard, Poppert Holger
Department of Neurology, Klinikum rechts der Isar, Technische Universität, Munich, Germany.
Acta Neurol Belg. 2009 Mar;109(1):44-8.
Whereas extraintestinal manifestations of inflammatory bowel disease in general are quite common, cerebral vasculitis is considered a very rare condition. We present a case of Crohn's disease-associated vasculitis mimicking migraine with aura.
A 28-year-old woman with Crohn's disease and known migraine with aura had suffered from daily migraine attacks with recurrent focal neurological deficits for 6 weeks. Cerebral magnetic resonance imaging showed multiple acute, subacute, and chronic ischemic lesions in different vascular territories. Magnetic resonance and computed tomography angiography demonstrated vessel changes consistent with cerebral vasculitis. Laboratory investigations revealed systemic inflammation and lymphomonocytic pleocytosis of cerebrospinal fluid, supporting the diagnosis of Crohn's disease-associated vasculitis. Symptoms and inflammatory parameters quickly normalized after high-dose prednisolone treatment. During immunosuppressive therapy, migraine recurred only once in 11 months.
Cerebral vasculitis is a very rare but severe complication in Crohn's disease and should be excluded in case of comorbidity with migraine with aura. In our patient, migraine with aura may have been the only symptom of cerebral vasculitis for several years.
虽然炎症性肠病的肠外表现总体上相当常见,但脑血管炎被认为是一种非常罕见的病症。我们报告一例克罗恩病相关血管炎,其症状类似伴有先兆的偏头痛。
一名28岁患有克罗恩病且已知患有伴有先兆偏头痛的女性,每日发作偏头痛,并伴有复发性局灶性神经功能缺损,持续6周。脑部磁共振成像显示在不同血管区域有多个急性、亚急性和慢性缺血性病变。磁共振血管造影和计算机断层血管造影显示血管变化符合脑血管炎表现。实验室检查显示全身炎症以及脑脊液淋巴细胞增多,支持克罗恩病相关血管炎的诊断。大剂量泼尼松龙治疗后,症状和炎症指标迅速恢复正常。在免疫抑制治疗期间,偏头痛在11个月内仅复发一次。
脑血管炎是克罗恩病中一种非常罕见但严重的并发症,在合并伴有先兆偏头痛的情况下应予以排除。在我们的患者中,伴有先兆的偏头痛可能多年来一直是脑血管炎的唯一症状。