Actionable diagnosis of neuroleptospirosis by next-generation sequencing.
A 14-year-old boy with severe combined immunodeficiency presented three times to a medical facility over a period of 4 months with fever and headache that progressed to hydrocephalus and status epilepticus necessitating a medically induced coma. Diagnostic workup including brain biopsy was unrevealing. Unbiased next-generation sequencing of the cerebrospinal fluid identified 475 of 3,063,784 sequence reads (0.016%) corresponding to leptospira infection. Clinical assays for leptospirosis were negative. Targeted antimicrobial agents were administered, and the patient was discharged home 32 days later with a status close to his premorbid condition. Polymerase-chain-reaction (PCR) and serologic testing at the Centers for Disease Control and Prevention (CDC) subsequently confirmed evidence of Leptospira santarosai infection.
Duke Scholars
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Related Subject Headings
- Severe Combined Immunodeficiency
- Sequence Analysis, DNA
- Meningoencephalitis
- Male
- Leptospirosis
- Leptospira
- Humans
- Headache
- General & Internal Medicine
- Fever
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Severe Combined Immunodeficiency
- Sequence Analysis, DNA
- Meningoencephalitis
- Male
- Leptospirosis
- Leptospira
- Humans
- Headache
- General & Internal Medicine
- Fever