Alice in Wonderland Syndrome as a Rare Presentation of Cryptogenic Stroke: A Case Report
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Updated: Jul 19, 2026

Portable Thermographic Screening for Detection of Acute Wallenberg's Syndrome
Published on: September 19, 2019
Saba Ahmed1, Samreen Ahmed1, Jawad Zafar2
1College of Medicine, Saint James School of Medicine, Arnos Vale, VCT.
Abstract:
Alice in Wonderland syndrome (AIWS) is a rare neurological disorder characterized by perceptual distortions, including alterations in body image perception and time perception. This case report presents a 94-year-old female patient who exhibited visual and auditory hallucinations, including macropsia (perception of objects as larger than their actual size), suggestive of AIWS, following an ischemic stroke. Despite initial suspicions of AIWS, imaging revealed chronic infarcts in the posterior right parietal lobe and the left occipital lobe, suggesting a stroke etiology. Management focused on symptomatic treatment with quetiapine, which effectively alleviated visual and auditory hallucinations, paranoia, and psychosis. This case explores the importance of thorough diagnostic evaluation to distinguish between post-stroke hallucinations versus those associated with AIWS. Additionally, it highlights the need for further research to expand on the mechanisms and optimal management strategies for AIWS, particularly in the context of stroke and other neurological conditions.
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