Chronic cyanosis since infancy: Unveiling a giant right pulmonary arteriovenous malformation

Dian Komalaa, Harry Galuh Nugrahaa, Firman Ramadhana, Rais Khairuddina, Rahmat Budi Kuswiyantob, Putria Rayani Apandi
Universitas Padjadjaran.
Indonesia

Radiology Case Reports
Radiol Case Rep 2025; 20: 5353-5356
DOI: 10.1016/j.radcr.2025.06.084

Abstract
Giant pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies involving direct connections between pulmonary arteries and veins, leading to right-to-left shunting and systemic hypoxemia. While small PAVMs may be asymptomatic, larger lesions often present with dyspnea, cyanosis, and related complications. An 18-year-old female with progressive dyspnea and cyanosis-first noted during infancy-was found to have a giant PAVM in the right lower lung lobe on thoracic computed tomography (CT). Imaging, particularly computed tomography (CT), was essential for diagnosis and treatment planning. This case underscores the need to consider PAVMs in the differential diagnosis of chronic cyanosis and highlights the critical role of radiologists in identifying and characterizing these lesions to guide appropriate management.and characterizing these lesions to support optimal clinical decision-making.

Category
Pulmonary Arteriovenous Malformations
Symptoms and Findings Associated with Pulmonary Vascular Disease
Diagnostic Testing for Pulmonary Vascular Disease. Non-invasive Testing

Age Focus: Pediatric Pulmonary Vascular Disease

Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication

Article Access
Free PDF File or Full Text Article Available Through PubMed or DOI: Yes

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