PRES Induced by Cyclosporin with Normal Blood Concentrations in a Bone Marrow Recipient

R. Charfi, M. Bensassi, E. Gaïes, H. Eljebari, N. Jebabli, M. Lakhal, A. Klouz, I. Salouage, S. Trabelsi
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引用次数: 10

Abstract

Introduction: Posterior reversible encephalopathy syndrome (PRES) is a clinic neuroradiological entity. This syndrome occurs in complex conditions as allogenic bone marrow transplantation, organ transplantation and immunosuppressant therapy such as cyclosporin (CsA). The occurrence of PRES is favored by a high concentration of CsA. Therefore, therapeutic monitoring of CsA is necessary to effects due to overdose. The therapeutic range of CsA is between 150-300 ng/mL. We aimed to present a case PRES induced by CsA in bone marrow transplantation with normal cyclosporine blood concentrations. Case: A 26 years old man received an allogenic bone marrow for bone marrow aplasia in January 2013. He was treated by CsA. Mean CsA dose was 2.57 mg/kg/day. CsA mean blood concentration was 295 ng/mL. After 20 days, our patient presented a complex partial seizure and cortical abnormal. He had no history of head injury, epilepsy or hypertension and there was no family history of neurological or psychiatric disorders. Patient’s blood pressure wasn’t measured. CsA was stopped. He received mycophenolate acid and clonazepam. Seizure and abnormal vision vanished 10 days later. Whereas, the patient developed graft-versus-host disease (GVHD). Then, mycophenolate acid was stopped 1.5 month later and CsA taken back. CsA mean dose was 1.1 mg/kg/day. Mean CsA blood concentration was 167.71 ng/mL. After two months, the patient developed general seizures and in Magnetic Resonance Imaging (MRI) there was a low-density in the subcortical white matter areas. So, CsA was stopped once and for all and the seizures vanished few days later. Conclusion: PRES is responsible for various and no specific neurological symptoms. These symptoms are usually reversible but sometimes fatal. Therapeutic monitoring of CsA was necessary to avoid neurotoxicity depending of concentration but we must remain cautious even if patients have CsA blood concentrations in the therapeutic range.
正常血药浓度环孢素诱导骨髓受体的PRES
后可逆性脑病综合征(PRES)是一种临床神经放射学疾病。这种综合征发生在异体骨髓移植、器官移植和免疫抑制治疗如环孢素(CsA)等复杂情况下。高浓度的CsA有利于PRES的发生。因此,对CsA的治疗监测是必要的,因为过量的影响。CsA的治疗范围在150-300 ng/mL之间。我们的目的是报道一例环孢素血药浓度正常的骨髓移植中CsA诱导的PRES。病例:一名26岁男性于2013年1月因骨髓发育不全接受同种异体骨髓移植。经CsA治疗。CsA平均剂量为2.57 mg/kg/d。CsA平均血药浓度为295 ng/mL。20天后,我们的病人出现了复杂的部分癫痫发作和皮层异常。患者无颅脑损伤史、癫痫史、高血压史,无神经或精神疾病家族史。没有测量病人的血压。CsA停止了。他接受了霉酚酸和氯硝西泮。10天后癫痫发作和视力异常消失。然而,患者出现了移植物抗宿主病(GVHD)。1.5个月后停用霉酚酸,重新服用CsA。CsA平均剂量为1.1 mg/kg/d。CsA血药浓度平均为167.71 ng/mL。两个月后,患者出现一般性癫痫发作,磁共振成像(MRI)显示皮质下白质区低密度。所以,CsA被一劳永逸地停止了,几天后癫痫发作消失了。结论:PRES可引起多种神经系统症状,但无特异性。这些症状通常是可逆的,但有时是致命的。CsA的治疗监测是必要的,以避免根据浓度的神经毒性,但我们必须保持谨慎,即使患者的CsA血药浓度在治疗范围内。
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