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vol.27 suppl.2Onset of primary Sjögren syndrome with mitochondrial polymyositis, axonal neuropathy, and hypokalaemic paralysis: Case report índice de autoresíndice de assuntospesquisa de artigos
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Revista Colombiana de Reumatología

versão impressa ISSN 0121-8123

Resumo

HUERTA-ROSARIO, Andrely et al. Chronic meningitis as an initial presentation of Sjögren syndrome. Rev.Colomb.Reumatol. [online]. 2020, vol.27, suppl.2, pp.166-170.  Epub 10-Set-2021. ISSN 0121-8123.  https://doi.org/10.1016/j.rcreu.2020.06.016.

Sjögren syndrome (SS) is an autoimmune disease, rarely affecting the central nervous system. The case is reported on a 68-year-old male patient who presented with keratocon-junctivitis sicca and xerostomia, during neuropsychological evaluation showed moderate to severe multidomain cognitive impairment. The magnetic resonance showed evidence of hypertrophic pachymeningitis. The CSF study showed pleocytosis, mild proteinuria, and negative cultures. The immune positive profile, Anti SS-A, SS-B and salivary gland biopsy was compatible with SS. The treatment was started with methylprednisolone pulses at a dose of 1g every 24 h for three days, and controlled with maintenance therapy, showing a favorable response. Chronic meningitis is a diagnostic challenge; among the less common causes is hypertrophic pachymeningitis in SS, and less frequently in male patients (1/9). Non-specific neurological manifestations should be considered, such as headaches or neuropsychiatric symptoms, as on some occasions rare cases may be encountered, such as the one described.

Palavras-chave : Meningitis; Hypertrophic pachymeningitis; Sjögren's syndrome.

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