Dammeier Nele, Schubert Victoria, Hauser Till-Karsten, Bornemann Antje, Bischof Felix
University Tübingen, Center of Neurology and Hertie Institute for Clinical Brain Research, Hoppe-Seyler Strasse 3, 72076, Tübingen, Germany.
University Tübingen, Diagnostic and interventional Neuroradiology, Hoppe-Seyler Strasse 3, 72076, Tübingen, Germany.
BMC Neurol. 2015 Jul 8;15:108. doi: 10.1186/s12883-015-0363-8.
Progressive multifocal leukoencephalopathy is a severe demyelinating disease caused by the polyoma JC virus in patients with reduced immunocompetence. A few cases of progressive multifocal leukoencephalopathy have been reported in patients treated with fumaric acid esters.
A 53-year-old Caucasian woman reported to our clinic with a first focal epileptic seizure and mild cognitive impairment. Since 1.5 years, she was treated with fumaderm for her psoriasis. During that time, her lymphocyte counts ranged between 450 and 700/μl. Cerebral magnet resonance imaging showed multifocal subcortical T2 hyperintense lesions with partial gadolinium enhancement. She did not have antibodies against human immunodeficiency virus 1 and 2 and cerebrospinal fluid-polymerase chain reaction for viral infections including a sensitive JC-virus polymerase chain reaction were negative. The diagnosis of progressive multifocal leukoencephalopathy was established by histological analysis and detection of JC-virus desoxyribonucleic acid in brain biopsy specimens. Dimethyl fumarate was stopped and Mirtazapin and Mefloquin were initiated. Neurological examination and imaging remained stable.
Progressive multifocal leukoencephalopathy can occur in patients with lymphocyte counts between 450 and 700/μl, produce only faint symptoms and is not excluded by negative JC-virus-polymerase chain reaction in cerebrospinal fluid. The incidence of progressive multifocal leukoencephalopathy may thus be underestimated and a more careful surveillance of patients would be necessary.
进行性多灶性白质脑病是一种由多瘤JC病毒引起的严重脱髓鞘疾病,发生于免疫功能低下的患者。已有少数接受富马酸酯治疗的患者发生进行性多灶性白质脑病的病例报道。
一名53岁的白种女性因首次局灶性癫痫发作和轻度认知障碍前来我院就诊。1.5年来,她一直使用富马酸二甲酯治疗银屑病。在此期间,她的淋巴细胞计数在450至700/μl之间。脑磁共振成像显示多灶性皮质下T2高信号病变,部分钆增强。她没有抗人类免疫缺陷病毒1型和2型抗体,包括敏感的JC病毒聚合酶链反应在内的病毒感染的脑脊液聚合酶链反应均为阴性。通过组织学分析和脑活检标本中JC病毒脱氧核糖核酸的检测确诊为进行性多灶性白质脑病。停用富马酸二甲酯,开始使用米氮平和甲氟喹。神经学检查和影像学检查结果保持稳定。
淋巴细胞计数在450至700/μl之间的患者可能发生进行性多灶性白质脑病,仅产生轻微症状,脑脊液JC病毒聚合酶链反应阴性不能排除该病。因此,进行性多灶性白质脑病的发病率可能被低估,有必要对患者进行更仔细的监测。