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Published on: November 4, 2015
Acute Right Ventricular Dysfunction Secondary to Hereditary Angioedema Exacerbation
Abbas Shahmohammadi1, Kathryn M Burtson2
1Division of Pulmonary, Critical Care, and Sleep Medicine, University of Florida, Gainesville, USA.
A woman with hereditary angioedema (HAE) experienced acute right ventricular dysfunction. Symptoms resolved with HAE management, and cardiac function normalized on follow-up.
Area of Science:
- Cardiology
- Genetics
- Internal Medicine
Background:
- Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of severe swelling.
- Right ventricular dysfunction can occur in various cardiovascular conditions, but its association with HAE exacerbations is not well-documented.
Observation:
- A 31-year-old woman with a history of HAE presented with acute abdominal pain and swelling.
- Initial investigations revealed sinus tachycardia, T wave inversions, and elevated troponin levels.
- Echocardiography demonstrated dilated and severely hypokinetic right ventricle with normal left ventricular function.
Findings:
- The patient's symptoms, including abdominal swelling and elevated troponins, resolved with symptomatic management of her HAE exacerbation.
- Follow-up echocardiography six months later showed normalization of right ventricular function.
Implications:
- This case suggests a potential link between HAE exacerbations and acute right ventricular dysfunction.
- Further research is warranted to understand the pathophysiology and clinical significance of this association.
- Recognition of this potential complication may aid in the timely diagnosis and management of HAE patients presenting with cardiac symptoms.
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