Idiopathic Pulmonary Arteriovenous Malformation: A Case Report

Pulmonary arteriovenous malformation (PAVM) is a rare abnormal connection between a pulmonary vein and a pulmonary artery, resulting in blood bypassing the capillary bed and causing right-to-left shunting. We aim to report a case of idiopathic PAVM managed with coil embolization to highlight this rare disease. A 15-year-old girl presented with a 2-year history of progressively worsening shortness of breath on exertion and intermittent self-limiting hemoptysis. She had cyanosis with an oxygen saturation of 86% on room air. No telangiectasia was seen. Chest X-ray revealed nonhomogeneous opacifications, most marked in the right lower zone. High-resolution computed tomography (HRCT) chest demonstrated centrilobular nodules, some with a branching pattern in the anterior segment of the right upper lobe and apical segments of both the right upper and lower lobes; interlobar and intralobar septal thickening along with a prominent bronchovascular bundle in the right upper and lower lobes. CT pulmonary angiography revealed multiple dilated and enlarged serpiginous vessels in the right lung; in the arterial phase, simultaneous opacification of arteries and veins demonstrated a connection between the pulmonary artery and veins, consistent with the diffuse type of PAVM. A diagnosis of idiopathic diffuse PAVM was made, and three sessions of coil embolization were performed over a period of 1 year. By the 12-month follow-up, she was stable and asymptomatic. PAVM is a rare occurrence, and early screening with prompt management is required to improve prognosis. Our patient, who presented with shortness of breath and hemoptysis, was diagnosed with idiopathic PAVM. She refused surgery and was managed with coil embolization, which resulted in marked improvement. The differential diagnosis of shortness of breath includes respiratory, cardiac, and hematological diseases. A high index of clinical suspicion is required to timely diagnose PAVM to reduce complications and morbidity. PAVM is best managed by a multidisciplinary team encompassing an internist, pulmonologist, interventional radiologist, and cardiothoracic surgeon.

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Publication Details

Journal
Indian Journal of Respiratory Care
Published
2024-09-30
DOI
https://doi.org/10.5005/jp-journals-11010-1128
Primary Topic
Vascular Anomalies and Treatments
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article
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article

Idiopathic Pulmonary Arteriovenous Malformation: A Case Report

Muhammad Sohail Ajmal Ghoauri, Ayesha Zahid, Nauman Ismat Butt, Abdul Samad et al.
Indian Journal of Respiratory Care
Vascular Anomalies and Treatments
article

Idiopathic Pulmonary Arteriovenous Malformation: A Case Report

Muhammad Sohail Ajmal Ghoauri, Ayesha Zahid, Nauman Ismat Butt, Abdul Samad, Farah Naz, Zunaira Ashraf
article en

Abstract

Pulmonary arteriovenous malformation (PAVM) is a rare abnormal connection between a pulmonary vein and a pulmonary artery, resulting in blood bypassing the capillary bed and causing right-to-left shunting. We aim to report a case of idiopathic PAVM managed with coil embolization to highlight this rare disease. A 15-year-old girl presented with a 2-year history of progressively worsening shortness of breath on exertion and intermittent self-limiting hemoptysis. She had cyanosis with an oxygen saturation of 86% on room air. No telangiectasia was seen. Chest X-ray revealed nonhomogeneous opacifications, most marked in the right lower zone. High-resolution computed tomography (HRCT) chest demonstrated centrilobular nodules, some with a branching pattern in the anterior segment of the right upper lobe and apical segments of both the right upper and lower lobes; interlobar and intralobar septal thickening along with a prominent bronchovascular bundle in the right upper and lower lobes. CT pulmonary angiography revealed multiple dilated and enlarged serpiginous vessels in the right lung; in the arterial phase, simultaneous opacification of arteries and veins demonstrated a connection between the pulmonary artery and veins, consistent with the diffuse type of PAVM. A diagnosis of idiopathic diffuse PAVM was made, and three sessions of coil embolization were performed over a period of 1 year. By the 12-month follow-up, she was stable and asymptomatic. PAVM is a rare occurrence, and early screening with prompt management is required to improve prognosis. Our patient, who presented with shortness of breath and hemoptysis, was diagnosed with idiopathic PAVM. She refused surgery and was managed with coil embolization, which resulted in marked improvement. The differential diagnosis of shortness of breath includes respiratory, cardiac, and hematological diseases. A high index of clinical suspicion is required to timely diagnose PAVM to reduce complications and morbidity. PAVM is best managed by a multidisciplinary team encompassing an internist, pulmonologist, interventional radiologist, and cardiothoracic surgeon.

Indian Journal of Respiratory CareVol. 13(3)
Openalex Percentile: Top 71%
Vascular Anomalies and Treatments
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