Key result
A young woman presented with a rare, painless Stanford Type A aortic dissection manifesting as stroke-like symptoms and Horner's syndrome, which was managed conservatively but resulted in death.
Why the study?
Aortic dissection can present atypically, which complicates diagnosis and management.
Case Report (n=1)
This case highlights that Stanford Type A aortic dissection can present atypically with neurological symptoms and Horner's syndrome without chest pain, particularly in young patients with methamphetamine use.
Neurological presentations without chest pain may signal Type A dissection in young methamphetamine users; this case leaves open optimal management timing.
Aortic dissection is a rare cardiovascular emergency that can present atypically, complicating diagnosis and management. We report the case of a woman in her 30s with Stanford Type A aortic dissection, presenting with stroke-like symptoms and Horner's syndrome without chest pain. Initial management focused on her neurological deficits, delaying the diagnosis. Bedside echocardiography and confirmatory imaging ultimately revealed an extensive dissection. Despite medical management, the patient succumbed to her condition. This case underscores the importance of recognizing atypical presentations of aortic dissection to enable timely diagnosis and improve outcomes.
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Edwards et al. (2025) conducted a case report in Stanford Type A aortic dissection (n=1). Methamphetamine use was evaluated. A young woman presented with a rare, painless Stanford Type A aortic dissection manifesting as stroke-like symptoms and Horner's syndrome, which was managed conservatively but resulted in death.
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