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BMJ Case Rep ; 20172017 Aug 09.
Article in English | MEDLINE | ID: mdl-28794091

ABSTRACT

Unilateral absent right pulmonary artery is a rare developmental anomaly that usually presents in late childhood and adolescence as recurrent respiratory tract infections, dyspnoea and haemoptysis. We report a case of a 2-day-old baby with respiratory distress and differential cyanosis. Echocardiogram showed pulmonary hypertension with absent right pulmonary artery. The findings were confirmed by CT angiogram. The baby improved with pulmonary vasodilators and antifailure medications.


Subject(s)
Hypertension, Pulmonary/diagnosis , Pulmonary Artery/abnormalities , Respiratory System Abnormalities/diagnosis , Computed Tomography Angiography , Cyanosis/etiology , Diagnosis, Differential , Echocardiography , Humans , Hypertension, Pulmonary/diagnostic imaging , Hypertension, Pulmonary/drug therapy , Infant, Newborn , Male , Pulmonary Artery/diagnostic imaging , Respiratory System Abnormalities/diagnostic imaging , Sildenafil Citrate/administration & dosage , Sildenafil Citrate/therapeutic use , Vasodilator Agents/administration & dosage , Vasodilator Agents/therapeutic use
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