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Unilateral absent pulmonary artery (UAPA) is a congenital abnormality rarely diagnosed in adults. UAPA has a myriad of clinical presentations and pulmonary hypertension is present in a quarter of all cases. Isolated UAPA commonly affects the right pulmonary artery and occurs as a result of abnormal development of the sixth aortic arch segment. Due to its rarity, it remains a diagnostic and therapeutic challenge. We describe a case of UAPA in an adult presenting with severe pulmonary hypertension. We describe the appropriate diagnostic approach to a patient with pulmonary hypertension and illustrate the importance of a detailed evaluation to determine the underlying aetiology, particularly in rare causes. Furthermore, we review the clinical presentation, diagnosis and management challenges of UAPA in adults.

More information Original publication

DOI

10.1016/j.rmcr.2017.09.004

Type

Journal article

Publication Date

2017-01-01T00:00:00+00:00

Volume

22

Pages

238 - 242

Total pages

4

Keywords

CTEPH, Chronic thromboembolic pulmonary hypertension, CTPA, Computed tomography pulmonary angiogram, Diagnosis, ECG, Electrocardiogram, MRI, Magnetic resonance imaging, Pulmonary hypertension, SVT, Supraventricular tachycardia, Therapy, UAPA, Unilateral absent pulmonary artery, Unilateral absent pulmonary artery