스테로이드 저항성 신증후군 환아에서 사이클로스포린 투여 중 발생한 후두엽 가역성 뇌병증 증후군 1례 |
정민희, 이주훈, 염미선, 고태성, 박영서 |
1울산대학교 의과대학 아산병원 소아과 2울산대학교 의과대학 아산병원 소아과 3울산대학교 의과대학 아산병원 소아과 4울산대학교 의과대학 아산병원 소아과 5울산대학교 의과대학 아산병원 소아과 |
A Case of Posterior Reversible Encephalopathy Syndrome during Cyclosporine Therapy in a Child with Steroid Resistant Nephrotic Syndrome |
Min-Hee Jeong, Joo-Hoon Lee, Mi-Sun Yum, Tae-Sung Ko, Young-Seo Park |
1Department of pediatrics, Asan Medical Center, College of Medicine University of Ulsan 2Department of pediatrics, Asan Medical Center, College of Medicine University of Ulsan 3Department of pediatrics, Asan Medical Center, College of Medicine University of Ulsan 4Department of pediatrics, Asan Medical Center, College of Medicine University of Ulsan 5Department of pediatrics, Asan Medical Center, College of Medicine University of Ulsan |
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ABSTRACT |
The posterior reversible encephalopathy syndrome(PRES) is characterized clinically by a combination of acute or subacute confusion, lethargy, visual disturbance, and seizures. PRES has been described in various clinical settings, including severe hypertension, chemotherapy, eclampsia, and seizure. We report a case of a 7-year-old girl who had taken cyclosporine for steroid resistant nephrotic syndrome. Twenty one days after the cyclosporine therapy, she was admitted due to generalized tonic clonic seizure and headache. Her blood pressure was 170/90 mmHg. Magnetic resonance(MR) imaging showed necrotic/cystic lesions involving the bilateral parieto-occipital region. After discontinuation of cyclosporine, and control of blood pressure, she had no more seizure and headache. The follow-up MR examination which was performed 6 months later showed the decreased extent of the lesion. |
Key words:
Steroid resistant nephrotic syndrome | Posterior reversible encephalopathy syndrome | Cyclosporine |
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