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Primary angioplasty in CADASIL
Cherukupalli Raghu1, Christophe Loubeyre, Edouard Obadia
1Insitut Cardiovasculaire Paris Sud, Quincy-sous-Sénart, France.
Insights
A young patient with cerebral autosomal dominant arteriopathy with sub-cortical infarcts and leucoencephalopathy (CADASIL) experienced an acute coronary event. The condition was successfully managed with primary angioplasty and direct stenting, highlighting CADASIL
Area of Science:
- Cardiovascular Medicine
- Neurology
- Genetics
Background:
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (CADASIL) is a rare genetic disorder.
- CADASIL primarily affects small blood vessels in the brain, leading to neurological deficits.
- Cardiac manifestations in CADASIL are less commonly reported but significant.
Observation:
- An acute coronary event occurred in a young patient diagnosed with CADASIL.
- The patient presented with symptoms indicative of myocardial ischemia.
- This case highlights a potential, albeit rare, cardiovascular complication in CADASIL.
Findings:
- The acute coronary event in the CADASIL patient was successfully treated with primary angioplasty and direct stenting.
- The intervention restored coronary blood flow and relieved ischemic symptoms.
- This demonstrates the feasibility of interventional cardiology in managing cardiac events in CADASIL patients.
Implications:
- Coronary artery disease should be considered in the differential diagnosis of young CADASIL patients presenting with cardiac symptoms.
- Understanding the pathophysiology of CADASIL may shed light on its vascular complications beyond the brain.
- Timely and appropriate cardiovascular intervention can be effective in managing acute coronary events in this patient population.
Abstract:
We report an acute coronary event in a young patient suffering from cerebral autosomal dominant arteriopathy with sub-cortical infarcts and leucoencephalopathy (CADASIL) successfully treated by primary angioplasty and direct stenting. Coronary involvement and pathophysiology of this genetic disorder is discussed.
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