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Updated: Sep 5, 2025

Transient Middle Cerebral Artery Occlusion Model of Neonatal Stroke in P10 Rats
Published on: April 21, 2017
Infantile ischemic stroke secondary to profound arteriopathy
Shubhi G Goli1, Ria Pal2, Sarah Lee2,3
1Department of Emergency Medicine Stanford University School of Medicine Stanford University Stanford California USA.
Insights
Pediatric arterial ischemic stroke (AIS) is rare in emergency departments. Early recognition of subtle symptoms in infants is crucial for timely diagnosis and better outcomes.
Area of Science:
- Neurology
- Pediatrics
- Emergency Medicine
Background:
- Pediatric arterial ischemic stroke (AIS) is an uncommon emergency department (ED) presentation, often challenging to diagnose.
- Infants may present with non-specific symptoms like irritability and feeding difficulties, mimicking other conditions.
Observation:
- A 4-month-old female presented with irritability and feeding issues, progressing to neurologic deficits including gaze and tongue deviation.
- Imaging revealed a large right-sided cerebral infarct with diffuse extra- and intracranial vessel narrowing and tortuosity.
Findings:
- Despite a comprehensive workup including echocardiogram and extensive laboratory testing, the etiology of the pediatric AIS remained undetermined.
- The case underscores diagnostic challenges in pediatric AIS due to low clinical suspicion and non-specific presentations.
Implications:
- Maintaining high clinical suspicion for pediatric AIS is vital for early diagnosis and intervention.
- Prompt recognition and appropriate neuroimaging can lead to earlier neuroprotective measures and improved patient outcomes.
Abstract:
Pediatric arterial ischemic stroke (AIS) is an uncommon emergency department (ED) presentation. We share the case of a 4-month-old female with a chief complaint of irritability and difficulty feeding. During ED evaluation, she developed lateral gaze deviation, tongue deviation, and rhythmic leg movements. Computed tomography of the head revealed a right-sided hypodensity concerning for ischemic infarct without hemorrhagic conversion. Subsequent brain magnetic resonance imaging and arteriography confirmed a large right-sided cerebral infarct and demonstrated narrowing and tortuosity of almost all extra- and intracranial vessels. Comprehensive pediatric AIS workup, including echocardiogram and laboratory tests for anemia, hypercoagulability, inflammatory, and genetic panels, were non-diagnostic. This case highlights the difficulty in diagnosis of pediatric AIS due to low clinical suspicion, limited neurologic examination, and non-specific presentations that may suggest stroke mimics. Maintenance of clinical suspicion and early recognition of pediatric AIS can result in earlier initiation of neuroprotective measures and optimization of imaging strategies for better outcomes.
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