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Basal Ganglia Ischemic Stroke as Sentinel Sign for Pediatric Tuberculous Meningitis in an Immunocompetent Child: A
Albina Ponosheci Biçaku1,2, Kurtesh Sherifi3, Ardian Biçaku4
1Department of Infectious Diseases, Faculty of Medicine, University of Prishtina, Str. Bulevardi i Dëshmorëve, 10000 Prishtina, Kosovo.
Insights
Pediatric tuberculous meningitis (TBM) is difficult to diagnose, even in vaccinated children, often requiring neuroimaging and high clinical suspicion for early detection and treatment to prevent severe outcomes.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Medical Case Studies
Background:
- Tuberculous meningitis (TBM) is a severe form of tuberculosis in children, associated with high mortality and neurological deficits.
- Early diagnosis of TBM is complicated by nonspecific symptoms and a gradual onset.
Background:
Tuberculous meningitis (TBM) is the most severe manifestation of tuberculosis in children, with high mortality rates and long-term neurological sequelae. Early diagnosis is challenging due to its nonspecific symptoms and insidious onset.
Case Presentation:
An 8-year-old previously healthy male, fully vaccinated, presented with a two-week history of fever, headache, vomiting, and abdominal pain. Cerebrospinal fluid (CSF) analysis revealed lymphocytic pleocytosis, elevated protein, and low glucose levels, while multiplex polymerase chain reaction (PCR) testing for bacteria and viruses yielded negative results. Brain computed tomography (CT) revealed mild ventricular dilation and pansinusitis. Empirical antibacterial and antiviral therapy were initiated; however, the patient subsequently experienced neurological deterioration, including cranial nerve deficits and hemiparesis. Brain magnetic resonance imaging (MRI) demonstrated acute infarctions of the basal ganglia, raising suspicion for TBM. Repeated CSF sampling and Xpert MTB/RIF assay confirmed infection with Mycobacterium tuberculosis. Anti-tuberculosis treatment was initiated in combination with adjunctive corticosteroids, anticonvulsant and anticoagulant therapies, and supportive care, including neurosurgical intervention for hydrocephalus. After 16 months of treatment, the patient showed clinical improvement but sustained left-sided hemiparesis, visual impairment, and cognitive deficits.
Conclusions:
This case highlights the diagnostic challenges of pediatric TBM in immunocompetent and Bacillus Calmette-Guérin (BCG)-vaccinated children, particularly in the presence of initially negative microbiological findings. It emphasizes the importance of maintaining a high index of clinical suspicion and the crucial supportive role of neuroimaging findings, as well as the earlier initiation of empirical TB therapy especially when epidemiological plausibility exists. Early recognition and intervention remain critical to reducing morbidity and mortality associated with this devastating disease.
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