Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, Guangzhou, China.
Department of Pathology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
BMC Neurol. 2024 Oct 11;24(1):384. doi: 10.1186/s12883-024-03902-x.
Progressive multifocal leukoencephalopathy (PML) is an often fatal disease of the central nervous system caused by opportunistic infection of John Cunningham Polyomavirus (JCV). There's still no antiviral therapeutic strategy which was generally recognized as effective. The prognosis may differ in patients with different pathological mechanisms and treatments. We aim to report the effectiveness of combined treatment of low-dose, long-term immunoglobulin and mirtazapine in a pathologically proved PML case.
A patient presented with progressive acalculia, right-left confusion and visual neglection was recorded. She received 10-year immunosuppressive therapy for dermatomyositis. White matter lesions located in bilateral parietal lobe and callosum area symmetrically in MR scanning. JC virus analysis and brain biopsy in left parietal lobe were performed. The number of JCV copies was 2595 in CSF and 282,809 in brain specimen. Abundant foamy macrophages and the lymphatic cells were obvious in immunohistochemistry staining. Few SV-40 positive JC infected cell and more CD4 + and CD68 + cells were predominant. Immunosuppressive drugs were terminated after being diagnosed as PML for positive JCV and pathological characteristics. In addition, immunoglobulin (5 g/day) and mirtazapine (45 mg/day) were used. JC virus in CSF decreased to 0 after treatment for 4 months and was still negative in June 2023. The clinical symptoms improved, and white matter lesions recovered significantly.
We demonstrated that the combination treatment of IVIG and mirtazapine was effective in PML. Low-dose, long-term immunoglobulin might regulate the immune status in our case with controlled inflammatory reaction instead of destructive virus spreading. The therapy may be a prospective option for PML.
进行性多灶性白质脑病(PML)是一种由机会性感染约翰·坎宁安多瘤病毒(JCV)引起的中枢神经系统常致命疾病。目前仍没有被普遍认为有效的抗病毒治疗策略。不同的病理机制和治疗方法可能会导致患者的预后不同。我们旨在报告在经病理证实的 PML 病例中,联合使用小剂量、长期免疫球蛋白和米氮平治疗的效果。
一名患者出现进行性计算障碍、左右混淆和视觉忽视。她因皮肌炎接受了 10 年的免疫抑制治疗。磁共振扫描显示双侧顶叶和胼胝体区对称的白质病变。进行 JCV 分析和左顶叶脑活检。CSF 中的 JCV 拷贝数为 2595,脑组织标本中为 282809。免疫组化染色显示大量泡沫状巨噬细胞和淋巴细胞明显。SV-40 阳性 JCV 感染细胞较少,CD4+和 CD68+细胞较多。诊断为 PML 后,阳性 JCV 和病理特征,停用免疫抑制药物。此外,使用免疫球蛋白(5g/天)和米氮平(45mg/天)。治疗 4 个月后,CSF 中的 JCV 降至 0,2023 年 6 月仍为阴性。临床症状改善,白质病变明显恢复。
我们证明了 IVIG 和米氮平联合治疗在 PML 中的有效性。小剂量、长期免疫球蛋白可能通过调节免疫状态而不是破坏病毒传播来控制炎症反应,在我们的病例中可能是一种有前景的选择。