Department of Paediatrics, Division of Paediatric Neurology, Ghent University Hospital, C. Heymanslaan 10, B-9000, Gent, Belgium.
Department of Radiology, Division of Paediatric Radiology, Ghent University Hospital, C. Heymanslaan 10, B-9000, Gent, Belgium.
Eur J Paediatr Neurol. 2019 Jan;23(1):222-227. doi: 10.1016/j.ejpn.2018.11.003. Epub 2018 Nov 14.
Arterial ischemic stroke is rare in childhood. Often, the diagnosis is made after considerable delay. A thorough workup to pinpoint the underlying etiology is necessary, as a correct diagnosis is the determining factor in treatment decision. In case of primary angiitis of the central nervous system, treatment with corticosteroids and immunosuppressive agents is indicated.
We described an eleven-year-old boy who presented at the age of six years with left hemiparesis and hemianopia. Cerebral imaging showed acute ischemia in the right posterior cerebral artery territory. Extensive workup was negative. In the following eight months, he had recurrent strokes on three separate occasions due to progressive arteriopathy involving multiple large- and medium-sized vessels. A presumed diagnosis of primary angiitis of the central nervous system was made. Pulse intravenous methylprednisolone therapy was started followed by oral prednisolone. After the fourth stroke, a six-month treatment with cyclophosphamide was given which was followed by maintenance treatment with azathioprine. Shortly after cessation of corticosteroids and cyclophosphamide the subject relapsed. Cyclophosphamide was restarted in combination with corticosteroids and subsequently replaced by mycophenolate mofetil. Under mycophenolate mofetil maintenance treatment combined with low-dose corticosteroids, the patient achieved disease control with a relapse-free period of more than four years.
A guideline for current treatment of relapsing central nervous system angiitis in childhood is missing in the literature. We describe a subject with multiple relapses despite treatment with corticosteroids and immunosuppressive agents, and stabilization of his clinical condition and of the radiological signs under mycophenolate mofetil treatment.
儿童中很少发生动脉缺血性脑卒中。通常,诊断要延迟很长时间才能做出。需要彻底检查以确定潜在病因,因为正确的诊断是治疗决策的决定因素。在中枢神经系统原发性血管炎的情况下,需要使用皮质类固醇和免疫抑制剂进行治疗。
我们描述了一名 11 岁男孩,他在 6 岁时出现左侧偏瘫和偏盲。脑部影像学显示右侧大脑后动脉区域急性缺血。广泛的检查结果均为阴性。在接下来的 8 个月中,由于涉及多个大中血管的进行性血管病变,他有 3 次不同的复发性中风。考虑到中枢神经系统原发性血管炎的可能性,开始了脉冲静脉内甲基强的松龙治疗,随后口服泼尼松龙。第四次中风后,给予环磷酰胺 6 个月治疗,随后给予硫唑嘌呤维持治疗。在停止使用皮质类固醇和环磷酰胺后不久,患者复发。重新开始使用环磷酰胺联合皮质类固醇,随后用霉酚酸酯代替。在霉酚酸酯维持治疗联合低剂量皮质类固醇治疗下,患者的疾病得到控制,无复发期超过 4 年。
目前针对儿童中枢神经系统复发性血管炎的治疗指南在文献中缺失。我们描述了一名患者尽管接受了皮质类固醇和免疫抑制剂治疗,但仍多次复发,在霉酚酸酯治疗下,其临床状况和影像学征象稳定。