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Pulmonary arteriovenous malformations presenting as difficult-to-control asthma: a case report
Marta Navratil1, Vinko Vidjak, Filip Rubić
1Reference Center for Clinical Allergology of the Ministry of Health and Social Welfare, Srebrnjak Children's Hospital, Srebrnjak 100, HR-10000, Zagreb, Croatia. marta.navratil@gmail.com.
Pulmonary arteriovenous malformations can mimic difficult-to-control asthma. This case highlights the importance of considering these vascular anomalies in asthma evaluations, especially when symptoms are refractory to treatment.
Area of Science:
- Vascular Medicine
- Pulmonary Medicine
- Genetics
Background:
- Pulmonary arteriovenous malformations (PAVMs) are rare but important in diagnosing common lung issues like hypoxemia and dyspnea.
- PAVMs can present as pulmonary nodules on imaging.
Purpose of the Study:
- To report a case of PAVMs presenting as refractory asthma.
- To emphasize the diagnostic challenge posed by PAVMs.
Main Methods:
- A case study of an 11-year-old boy with severe asthma.
- Diagnostic imaging included chest X-ray and CT angiography.
- Hereditary hemorrhagic telangiectasia was diagnosed clinically and genetically (endoglin gene mutation).
Main Results:
- CT angiography revealed bilateral pulmonary arteriovenous malformations.
- The patient received embolotherapy for the PAVMs.
- Successful clinical outcome was achieved post-treatment.
Conclusions:
- Pulmonary arteriovenous malformations can present atypically, mimicking refractory asthma.
- Early diagnosis and appropriate intervention, such as embolotherapy, are crucial for managing PAVMs.
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