Title of article :
Case Report: Unilateral Pulmonary Artery Agenesis Presenting with Massive Hemoptysis
Author/Authors :
ALTURKI, ABDULAZIZ Najran University - College of Medicine - Department of Internal Medicine, Saudi Arabia , ALKHALDY, HUSAIN Y. King Khalid University - College of Medicine - Department of Internal Medicine, Saudi Arabia , AZIZ, SHAHID King Khalid University - College of Medicine - Department of Internal Medicine, Saudi Arabia , WANI, JAVED I. King Khalid University - College of Medicine - Department of Internal Medicine, Saudi Arabia
From page :
597
To page :
599
Abstract :
Background: Congenital unilateral absence of a pulmonary artery is a rare anomaly most frequently accompanied by other cardiovascular anomalies. It is usually diagnosed during childhood and effectively treated surgically by doing a pneu-monectomy. Case Report: A young adult with right pulmonary artery agenesis, who presented in November 2011 to Aseer Central Hospital with massive hemoptysis. He was treated successfully with arterial embolization, as the definitive management plan was an elective pneumonectomy after referral to an expert specialized center for the latter form of treatment. Conclusion: Pulmonary artery agenesis, needs to be considered as a cause of recurrent hemoptysis, especially in a patient with decreased unilateral lung volume. Such patients should be strongly considered for undergoing a pulmonary angiography for confirming this rare pulmonary vascular malformation.
Keywords :
Massive hemoptysis , Unilateral agenesis , Pulmonary artery
Journal title :
The Medical Journal of Cairo University
Journal title :
The Medical Journal of Cairo University
Record number :
2540909
Link To Document :
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