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Published on: July 24, 2016
A rare infective cause of stroke in an immunocompetent child
Juhi Gupta1, Biswaroop Chakrabarty1, Gagandeep Singh2
1Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Insights
This case study highlights a rare fungal infection causing both venous and arterial stroke in an immunocompetent child. Early diagnosis and targeted antifungal treatment led to a full recovery, demonstrating effective management of sino-orbital aspergillosis.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Childhood stroke is frequently linked to infections, presenting with diverse symptoms.
- This report details a unique case of a child experiencing both venous and arterial stroke due to a rare infection.
Observation:
- A 12-year-old girl presented with fever, orbital cellulitis, and altered mental status.
- Neurological examination revealed ophthalmoparesis, facial palsy, and signs of meningeal irritation.
- Advanced neuroimaging demonstrated thrombosis in the cavernous sinus and internal carotid artery.
Findings:
- Cultures from nasal debridement identified Aspergillus flavus as the causative agent.
- Initial broad-spectrum antibiotics and anticoagulation were insufficient.
- Treatment with intravenous voriconazole resulted in rapid clinical and radiological improvement.
Implications:
- Early identification and targeted antifungal therapy are crucial for managing sino-orbital aspergillosis.
- Aggressive management, including surgical debridement when necessary, can lead to favorable outcomes despite the infection's severity.
- This case underscores the importance of investigating deep-seated infections unresponsive to standard treatment to identify the specific pathogen.
Background:
Infections are a common cause of childhood stroke with variable presentation. The current case describes a rare infective cause of venous and arterial stroke in an immunocompetent girl with management implications.
Case Description:
A 12 year old girl, presented with history of fever for 10 days, painful swelling of right eye for 7 days and altered sensorium for 2 days. On examination, she had right eye orbital cellulitis and fullness of right paranasal area. On nervous system examination, she was delirious, had right eye ophthalmoparesis, left upper motor neuron facial palsy and signs of meningeal inflammation. Her contrast enhanced CT head and subsequent MRI brain with arteriography and venography revealed right cavernous sinus and distal internal carotid artery thrombosis. She was started on intravenous ceftriaxone and vancomycin and subcutaneous heparin. In view of persistent symptoms, endoscopic debridement of right nasal cavity was done, which showed growth of aspergillus flavus. Subsequently, she was started on intravenous voriconazole. Within a week, she was afebrile, her inflammatory and neurological signs started improving. She was discharged after 3 weeks of intravenous voriconazole which was continued for 3 more weeks orally. Her procoagulant and immunodeficiency work up were normal. At 4 months follow up, she showed both clinical and radiological resolution.
Conclusions:
Despite high mortality described in sino-orbital aspergillosis, early and appropriate treatment led to optimal outcome. In deep seated infections, isolation of etiological organism should be attempted, particularly when patient doesn't respond to conventional antimicrobial therapy.
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