Abstract

Pulmonary artery aneurysms are rare entities usually associated with congenital anomalies that increase blood flow/pressure in the pulmonary circulation, like left to right shunts and/or severe pulmonary valve pathologies. Clear re-commendations about their management are lacking. We report on a case of severe congenital pulmonary valve stenosis associated with a giant pulmonary artery aneurysm, secondary right ventricular outflow tract obstruction and right to left atrial shunt. We discuss the diagnostic pathway, therapeutic approach and patient evolution. The case report proves that a complete imaging of the heart and blood vessels is mandatory with severe pulmonary valve stenosis, in order to better describe its repercussions on the right ventricle and pulmonary circulation. They might be under detected by simple tran-sthoracic echocardiography but their presence has important therapeutic implications.

Highlights

  • CASE PRESENTATIONRaluca Sosdean[1], Adina Ionac[1], Alina Stan[2], Sorin Pescariu[1], Adrian Ursulescu[1,2]

  • Pulmonary artery aneurysms (PAA) represent a dilation of the main pulmonary artery of more than 40mm[1]. They are very rare entities; studies show a prevalence of 0.007% with 89% in the pulmonary artery trunk[2]

  • Pulmonary stenosis has been asociated with elastic fibres deficiency in the pulmonary artery wall, predisposing to dissection during balloon valvuloplasty[6]

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Summary

CASE PRESENTATION

Raluca Sosdean[1], Adina Ionac[1], Alina Stan[2], Sorin Pescariu[1], Adrian Ursulescu[1,2]

INTRODUCTION
CONCLUSIONS

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