Bennett B, Booth T, Quan A
Children's Medical Center of Dallas, USA.
Clin Nephrol. 2003 Mar;59(3):196-200. doi: 10.5414/cnp59196.
Neurologic complications of hemolytic uremic syndrome, including seizures, usually occur early during the acute phase of the illness. We report a3-year-old girl with classic diarrhea-associated hemolytic uremic syndrome who developed late onset seizures, hemiparesis and transient blindness on the 17th hospital day, at which time her recovery was characterized by improvement in her blood pressure, serum electrolytes, renal function, hematocrit and platelet count. A CT and MR revealed brainstem and posterior parietal and occipital infarct/edema. The association of these radiologic findings within the posterior distribution along with visual loss and seizures are unique to posterior reversible encephalopathy syndrome. Within 7 days, she regained motor function and vision and had no further seizure activity. At 6 months follow-up, physical examination revealed normal motor function and vision and a repeat MR showed near resolution of the previous findings with minimal occipital lobe gliosis. This case report describes the uncommon finding of late onset seizures occurring during the recovery phase of hemolytic uremic syndrome with MR findings consistent with posterior reversible encephalopathy syndrome.
溶血尿毒综合征的神经系统并发症,包括癫痫发作,通常在疾病急性期的早期出现。我们报告一名3岁女童,患有典型的腹泻相关性溶血尿毒综合征,在住院第17天出现迟发性癫痫发作、偏瘫和短暂性失明,此时她的恢复表现为血压、血清电解质、肾功能、血细胞比容和血小板计数改善。CT和磁共振成像(MR)显示脑干、顶叶后部和枕叶梗死/水肿。这些沿后部分布的影像学表现与视力丧失和癫痫发作相关,是后部可逆性脑病综合征所特有的。7天内,她恢复了运动功能和视力,且未再有癫痫发作。在6个月的随访中,体格检查显示运动功能和视力正常,重复MR显示先前的表现几乎消退,仅枕叶有轻度胶质增生。本病例报告描述了溶血尿毒综合征恢复期出现迟发性癫痫发作这一罕见发现,其MR表现符合后部可逆性脑病综合征。