ArticleThe American journal of case reports2018
Pyogenic Ventriculitis and Meningitis Caused by Streptococcus Acidominimus in Humans: A Case Report.
Article in The American journal of case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 8 citations in OpenAlex.
- Primary Adult Ventriculitis due to Streptococcus pneumoniae with Obstructive Hydrocephalus: Role of Arachnoid Cyst as a Predisposing Factor.Annals of Indian Academy of Neurology · 2026Article
- Primary pyogenic ventriculitis caused by Streptococcal pneumoniae in adults.Journal of family medicine and primary care · 2019Article
- A Retrospective Study on the First Cerebrospinal Fluid Taken from External Ventricular Drainage Insertion in Meningitis Patients with Hydrocephalus.The Malaysian journal of medical sciences : MJMS · 2019Article
- Life-threatening pyogenic ventriculitis, complicating endocarditis, presenting as sudden hearing loss.Oxford medical case reports · 2019Article
- The Interleukin-10 Family of Cytokines and Their Role in the CNS.Frontiers in cellular neuroscience · 2018Review
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND Streptococcus acidominimus, which belongs to the viridans streptococci group, is rarely considered pathogenic in humans. However, over the past 10 years, this bacterium has been reported to cause serious infections in humans, particularly among the critically ill. This article is the first case report of pyogenic ventriculitis (PV) and meningitis caused by S. acidominimus in North America. CASE REPORT A 49-year-old Asian male presented to the emergency department with complaints of a headache, fever greater than 37.8°C (100°F) and confusion, of approximately 3 days duration. He was unable to speak coherently or follow approximately half of the given commands. He appeared ill; an intracranial infection was suspected. Magnetic resonance imaging of the brain showed: 1) infected proteinaceous material and pus-like material throughout the cerebral sulci and in the occipital horns of both lateral ventricles, 2) ependymal signal abnormality of the posterolateral margin of the occipital horn of the left lateral ventricle, and 3) early hydrocephalus suggestive of ventriculitis and meningitis. The blood and cerebrospinal fluid cultures were positive for S. acidominimus. The patient improved with minimal deficits after 6 weeks of IV ceftriaxone without requiring a neurosurgical intervention, such as an intraventricular drain or neuroendoscopic surgery. CONCLUSIONS PV and meningitis caused by S. acidominimus are rare but potentially fatal intracranial infections. Therefore, despite the risk of generalizing, our case report suggests that PV and meningitis caused by S. acidominimus can be effectively treated with a prompt and prolonged course of IV ceftriaxone without neurosurgical intervention.
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