ArticleThe Journal of infectious diseases2026
Cerebral Venous Thrombosis in Previously Healthy Patients with Cryptococcal Meningitis.
Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Review
- Admission D-Dimer for Early Risk Stratification of in-Hospital Mortality in Adults with Non-HIV Cryptococcal Meningitis: A Retrospective Cohort Study.Infection and drug resistance · 2026Article
Corrections and comments
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Authors and funding
13 authors.
Funding
Abstract
backgroundCerebral venous sinus thrombosis (CVST), though a recognized complication of cryptococcal meningitis (CM), has been rarely reported. This study investigates the clinical features of CVST in a retrospective cohort of previously healthy, non-HIV CM patients.
methodsWe reviewed medical records of 89 immunocompetent CM patients admitted between January 2005 and April 2024. CVST incidence, clinical course, neuroimaging, and laboratory data were analyzed. Genetic analysis was performed to detect thrombophilia-associated variants. To explore thrombosis-related gene expression during neuroinflammation, cerebrospinal fluid (CSF) cells collected at the time of cryptococcal post-infectious inflammatory response syndrome (cPIIRS) diagnosis were subjected to single-cell RNA sequencing.
resultsCVST occurred in 5.6% (CI 1.9%-12.6%) of CM patients, a rate comparable to bacterial CNS infections. No known pathogenic variants in known thrombophilia-associated genes were identified. However, 44 genes previously linked to thrombosis showed elevated expression-defined as ≥150 single-cell sequencing reads-in a cPIIRS patient.
conclusionsCVST is a potentially treatable complication of CM. MRI and MRV of the brain are valuable diagnostic tools. The absence of thrombophilia mutations suggests that neurologic infection itself contributes to thrombotic risk. Notably, CSF gene expression patterns may serve as biomarkers for CVST susceptibility. Future case-control studies may validate these findings and uncover genetic risk factors contributing to CVST.
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