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Case report: First case of Borrelia miyamotoi meningitis in an immunocompromised patient in Norway.

Authors :
Schwartz T
Hoornstra D
Øie E
Hovius J
Quarsten H
Source :
IDCases [IDCases] 2023 Jul 31; Vol. 33, pp. e01867. Date of Electronic Publication: 2023 Jul 31 (Print Publication: 2023).
Publication Year :
2023

Abstract

Background: Tick-borne disease caused by B. miyamotoi (BMD) usually manifest as a febrile illness in humans. Complications include relapsing fever and in rare occasions involvement of the central nervous system. Only a few cases of meningoencephalitis have been described, mostly in immunosuppressed patients.<br />Case Presentation: A 70-year-old female receiving immunosuppressive rituximab therapy presented with frontal headache, dizziness, nausea, vomiting and chills. Clinical laboratory blood analyses were normal. Cerebrospinal fluid (CSF) was translucent and analysis showed increased leucocyte count (187 10 <superscript>6</superscript> /L) and elevated level of protein (1056 mg/L). Empiric antibiotic treatment was initiated. The patient showed an early symptomatic relief and 24 h after admission she was discharged from the hospital and antibiotic treatment was discontinued. Two weeks after hospitalisation the B. miyamotoi specific PCR turned out positive in both CSF and serum. At the time, the patient was recovered with mild residual headache. She was treated with high dose doxycycline and her subtle symptoms disappeared.<br />Conclusions: To our knowledge, we present the first patient with BMD-associated meningitis in Norway, one of eight cases reported worldwide. The patient had mild symptoms and received an early diagnosis. A more severe progression or relapse of disease may have been prevented by antibiotic treatment. BMD should be considered as causes of aseptic meningitis, especially in immunosuppressed patients living in endemic areas.<br />Competing Interests: None.<br /> (© 2023 The Authors.)

Details

Language :
English
ISSN :
2214-2509
Volume :
33
Database :
MEDLINE
Journal :
IDCases
Publication Type :
Report
Accession number :
37577049
Full Text :
https://doi.org/10.1016/j.idcr.2023.e01867