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Pulmonary Arteriovenous Malformations: What the Interventional Radiologist Should Know
Claire S Kaufman1, Jamie McDonald2, Heather Balch3
1Dotter Department of Interventional Radiology, Pacific Northwest HHT Center of Excellence, Oregon Health & Sciences University, Portland, Oregon.
Pulmonary arteriovenous malformations (PAVMs) involve abnormal blood vessel connections in the lungs, often linked to hereditary hemorrhagic telangiectasia (HHT). Transcatheter embolization is the primary treatment for these shunts.
Area of Science:
- Vascular Medicine
- Pulmonology
- Genetics
Background:
- Pulmonary arteriovenous malformations (PAVMs) are abnormal direct connections between pulmonary arteries and veins.
- These shunts bypass the lung's capillary bed, leading to a right-to-left shunt.
- A significant majority (80-90%) of PAVMs are associated with hereditary hemorrhagic telangiectasia (HHT).
Purpose of the Study:
- To provide a comprehensive review of pulmonary arteriovenous malformations (PAVMs).
- To cover clinical presentation, diagnostic workup, and genetic associations.
- To detail the standard treatment of transcatheter embolization, including complications and follow-up.
Main Methods:
- Review of clinical presentation and symptoms.
- Discussion of diagnostic imaging findings.
- Analysis of transcatheter embolization as the standard of care.
Main Results:
- PAVMs can be asymptomatic or present with diverse symptoms including hypoxia, dyspnea, and migraines.
- Paradoxical embolization and rupture are potential severe sequelae.
- Transcatheter embolization is the established and effective treatment modality.
Conclusions:
- PAVMs, particularly those associated with HHT, require thorough evaluation and management.
- Transcatheter embolization is the current gold standard for treating PAVMs.
- Understanding PAVM presentation, genetics, and treatment is crucial for patient outcomes.
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