| Literature DB >> 29710027 |
Yumi Akagawa1, Akihiro Ueno1, Junji Ikeda1, Wataru Ishii2, Yukiko Shishido-Hara3, Yoshiki Sekijima1,4.
Abstract
Patient 1 was a 59-year-old woman receiving prednisolone for idiopathic hypereosinophilia. Brain MRI of patient 1 disclosed slight gadolinium enhancement at lesions, indicating inflammation. Patient 2 was a 32-year-old woman with systemic lupus erythematosus under immunosuppressive therapy. Brain biopsy of patient 2 showed balanced infiltration of CD8+ and CD4+ T lymphocytes at the sites of lesions. Both subjects were diagnosed as having progressive multifocal leukoencephalopathy (PML) shortly after the onset of neurological symptoms and were treated with a combination of mefloquine, mirtazapine, and risperidone. Both patients remain alive with improved neurological symptoms even after long-term follow-up (24 months in patient 1 and 45 months in patient 2). Although the prognosis of PML is very poor, our findings suggest that pharmacotherapy may be effective for patients with well-controlled immune reactions against the JC virus.Entities:
Keywords: JC virus; mefloquine; mirtazapine; progressive multifocal leukoencephalopathy; risperidone
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Year: 2018 PMID: 29710027 DOI: 10.5692/clinicalneurol.cn-001166
Source DB: PubMed Journal: Rinsho Shinkeigaku ISSN: 0009-918X