Case report of ADEM in an adult patient with chikungunya

Author:

Barros João Alfredo M. M.1ORCID,Vasconcelos Arthur Felipe Barbosa2ORCID,Carvalho Francisco Anderson de Sá2ORCID,Filho Gilmar Leite Pessoa2ORCID,Gomes Ana Luísa Castelo Branco2ORCID,Leite Raíssa N. L. F.3ORCID,Bezerra João Felipe4ORCID,Leite Juliana Magalhães2ORCID,Andrade Rafael de Souza2ORCID,Oliveira Bianca Etelvina Santos de5ORCID,Meira Alex T.12ORCID

Affiliation:

1. Departamento de Medicina Interna, Serviço de Neurologia Universidade Federal da Paraíba João Pessoa Brazil

2. Hospital Metropolitano Dom José Maria Pires, Serviço de Neurologia João Pessoa Brazil

3. Nova diagnóstico por imagem João Pessoa Brazil

4. Laboratório de Vigilância Molecular Aplicada (LAVIMAP) Universidade Federal da Paraíba João Pessoa Brazil

5. Centro de Referência em Esclerose Múltipla do Estado da Paraíba, CREM‐PB, Funad João Pessoa Brazil

Abstract

AbstractAcute Disseminated Encephalomyelitis (ADEM) is a demyelinating immune‐mediated disease characterized by bilateral and confluent lesions in white matter (WM), with an acute onset. This condition may arise due to a myriad of etiological factors, encompassing mainly vaccines and viral infections. This case report describes a 39‐y‐old patient who presented with a sudden onset of fever, confusion, and reduced level of consciousness, associated with paraparesis in the lower limbs and urinary retention, 2 d before admission to the neurological emergency department. The work‐up included analysis of the cerebrospinal fluid (CSF), which showed 1.6 cells/mm3 and elevated proteins (91 g/dL); in addition to magnetic resonance imaging (MRI) of the brain and the spinal cord, in which hyperintense ovoid lesions with asymmetrical and bilateral distribution in the WM and basal ganglia were observed in the T2 and FLAIR. Later, chikungunya virus was detected in a molecular viral panel in the CSF. The patient exhibited an improvement radiologically, and in his condition following pulse with methylprednisolone and intravenous immunoglobulin therapy, and 40 mg of prednisone was prescribed for management during outpatient follow‐up. This study highlights arbovirus infections as a possible cause of acute neurological conditions, involving both the brain and the spinal cord. Furthermore, the findings observed in the report were compared with those described in the literature, including other arboviruses. In conclusion, it was observed that the majority of patients responded to treatment with corticosteroids or immunoglobulins, with some neurological deficits eventually persisting. Therefore, more studies are needed to better investigate therapeutic options.

Publisher

Wiley

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