A Case Report of Progressive Multifocal Leukoencephalopathy in Peritoneal Dialysis

L. B. Lasfar, Y. Guedri, S. Mrabet, D. Zellama, A. Hassine, W. Sahtout, A. Azzebi, S. Toumi, A. Fradi, S. B. Ammou, A. Achour
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Abstract

We experienced a case manifesting progressive multifocal leucoencephalopathy (PML) in peritoneal dialysis (PD). A 27-year-old male patient had received a chronic PD therapy for 4 years. He had a past medical history of hypertension and myelodysplastic syndrome. He complained of hemiparesis with sudden onset and behavioral disorders. The patient seemed indifferent, incoherent with deficit walking. The cranial nerve examination showed a left central facial paralysis. Brain CT scan showed a paramedian right low density area not systemized, located in the corpus callosum and the centrum semiovale. Brain MRI confirmed the presence of PML by the detection of signal abnormalities in bilateral and asymmetrical white matter. The culture of cerebral spinal fluid was negative. The patient underwent six sessions of plasma exchange with favorable evolution. Few cases of PML have been reported in hemodialysis patients and no case has been previously described in PD. In our case, under immunocompromised conditions, precipitating factors appear multifactorial. Depressed immune system induced by chronic dialysis as well as liver disease and myelodysplasia might contribute to the development of florid clinical manifestation of PML. World J Nephrol Urol. 2017;6(3-4):35-39 doi: https://doi.org/10.14740/wjnu316w
腹膜透析进行性多灶性白质脑病1例报告
我们报告了一例腹膜透析(PD)患者表现为进行性多灶性白质脑病(PML)。一位27岁的男性患者接受了4年的慢性PD治疗。既往有高血压和骨髓增生异常综合征病史。他主诉有突然发作的偏瘫和行为障碍。病人似乎很冷漠,语无伦次,行走困难。颅神经检查显示左侧中枢性面瘫。脑部CT扫描显示右侧无系统低密度区,位于胼胝体和半椎体。脑MRI通过检测双侧和不对称白质信号异常证实PML的存在。脑脊液培养为阴性。患者接受了6次血浆置换治疗,进展良好。血液透析患者中很少有PML病例的报道,PD中也没有病例的报道。在我们的病例中,在免疫功能低下的情况下,诱发因素似乎是多因素的。慢性透析引起的免疫系统低下、肝脏疾病和骨髓增生异常可能是PML临床表现丰富的原因。世界肾脏病杂志,2017;6(3-4):35-39 doi: https://doi.org/10.14740/wjnu316w
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