Pulmonary arteriovenous malformations (PAVM) are abnormal communications between the pulmonary arteries and pulmonary veins. The large majority are congenital and are commonly associated with Rendu-Osler-Weber disease or hereditary haemorrhagic telangiectasia. The PAVM may remain asymptomatic or manifest with hypoxemia, hemoptysis, hemothorax and/or neurologic symptoms. Despite its low incidence, the PAVM represent a serious entity that must be taken into account since untreated patients are in risk and present a poor prognosis. Transcatheter embolization with coils or detachable balloons is currently accepted as the treatment of choice. We present 6 patients (5 women and one man) who underwent embolotherapy of PAVM showing the long-term clinical and radiological follow-up.