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Portable Thermographic Screening for Detection of Acute Wallenberg's Syndrome
Published on: September 19, 2019
Wallenberg Syndrome: An Exceptional Cause of Acute Vertigo in Children
Aude Ménétrey Ehresmann1, Hélène Cao Van2, Laura Merlini3
1Pediatric Neurology, Pediatric Subspecialties Service, Geneva Children's Hospital, Geneva, Switzerland.
Insights
A child
Area of Science:
- Pediatric Neurology
- Neuroscience
- Vascular Neurology
Background:
- Acute vertigo in children is diagnostically challenging.
- Central causes are uncommon but require prompt identification.
- Peripheral vestibular dysfunction is often the initial consideration.
Observation:
- A 7-year-old boy presented with acute rotary vertigo, nausea, and vomiting post-head trauma.
- Initial otoneurological evaluation did not confirm peripheral vestibular dysfunction.
- Subtle neurological signs prompted further investigation.
Findings:
- Brain MRI revealed a brainstem infarct in the medulla oblongata, consistent with Wallenberg syndrome.
- Vascular imaging was unremarkable, and no specific etiology was identified.
- Treatment with acetylsalicylic acid led to rapid vertigo resolution.
Implications:
- Brainstem infarcts should be considered in the differential diagnosis of acute vertigo in children.
- Thorough clinical examination is crucial for identifying subtle neurological deficits.
- Early recognition facilitates appropriate management and improves patient outcomes.
Abstract:
The assessment of acute vertigo in childhood is often challenging, but fortunately a central cause is rarely identified. We present the case of a 7-year-old boy who developed, after a mild head trauma, a rotary vertigo associated with nausea and vomiting. A posttraumatic peripheral vestibular dysfunction was first suspected but not confirmed by an otoneurological evaluation. When subtle neurological signs were elicited, a brain magnetic resonance imaging was promptly requested. This showed a small infarct on the lateral posterior left part of the medulla oblongata of the brainstem, typical of Wallenberg syndrome. Vascular imaging was normal and no defined etiology was found. The child was started on prophylactic acetylsalicylic acid. The rapid disappearance of vertigo was noted. On follow-up at 6 months, there has been no recurrence and neurological examination was fully normal. Our case extends the differential diagnosis of acute vertigo in childhood that rarely includes the possibility of a brainstem infarct whose recognition through appropriate clinical examination is nevertheless capital for appropriate investigations and management.
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