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Infante et al. Neuroimmunol Neuroinflammation 2017;4:211-5       Neuroimmunology and
           DOI: 10.20517/2347-8659.2016.52
                                                                                  Neuroinflammation

                                                                                                www.nnjournal.net
            Case Report                                                                         Open Access

           A case of atypical progressive multifocal

           encephalopathy mimicking acute ischemic

           stroke: case report and review of literature



           Maria Teresa Infante , Giovanni Novi , Riccarda Gentile , Laura Malfatto , Lucio Castellan , Carlo Serrati ,
                                                                                         3
                                                                          1
                             1
                                           1,2
                                                            1
                                                                                                      1
           Laura Barletta 3
           1 Neurology Unit, Department of Neurosciences, IRCCS San Martino IST, Largo Rosanna Benzi 10, 16132 Genoa, Italy.
           2 Department of Neurology, Ophtalmology, Genetics, Maternal and Child Health, University of Genoa, Largo Daneo 3, 16132 Genoa, Italy.
           3 Neuroradiology Unit, IRCCS San Martino IST, Largo Rosanna Benzi 10, 16132 Genoa, Italy.
           Correspondence to: Dr. Maria Teresa Infante, Neurology Unit, Deparment of Neurosciences, IRCCS San Martino IST, Largo Rosanna Benzi 10,
           16132 Genoa, Italy. E-mail: infante.mariateresa@gmail.com
           How to cite this article: Infante MT, Novi G, Gentile R, Malfatto L, Castellan L, Serrati C, Barletta L. A case of atypical progressive multifocal
           encephalopathy mimicking acute ischemic stroke: case report and review of literature. Neuroimmunol Neuroinflammation 2017;4:211-5.
                            Dr. Maria Teresa Infante is a young neurologist; she attended her neurology residency at Genoa’s University (Italy)
                            and she did her research especially in the field of neuroimmunology diseases.








                                         ABSTRACT
            Article history:              Progressive multifocal  encephalopathy  (PML) is a  rare  but  often  fatal  infectious  brain
            Received: 25 Nov 2016         disease caused by the reactivation of John Cunningham polyomavirus. Reactivation occurs
            Accepted: 10 Jul 2017         in immunocompromised  individuals with AIDS and leukemia,  on chemotherapy  or being
            Published: 19 Oct 2017        treated with immunosuppressant drugs (e.g. monoclonal antibodies). Cases of PML have been
                                          described in patients treated with natalizumab, efalizumab and rituximab used, respectively,
            Key words:                    for the treatment of (1) multiple sclerosis, (2) psoriasis and (3) haematological malignancies
            Progressive multifocal        or systemic autoimmune diseases (rheumatoid arthritis and systemic lupus erythematosus).
            encephalopathy,               The  authors describe  an unusual  case  of acute  brainstem  and cerebellar  PML following
            rituximab,                    chemotherapy for chronic lymphatic leukemia diagnosed 4 years before the onset of PML in
            immunosuppression             a 75-year-old man. The patient was treated with high dose chemotherapy and rituximab with
                                          complete response. The onset of symptoms of PML was very rapid and occurred after more
                                          than two years from last rituximab infusion; patient had a sudden neurological deterioration,
                                          with rapid progression to death in about a month from the onset of symptoms. Lesions were
                                          localized in the cerebellum, brainstem and such pattern has been reported in very few cases in
                                          the literature.

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