Congenital absence of the right pulmonary artery diagnosed by angiocardiography and cardiorespiratory studies

Madoff, Irving M.; Gaensler, Edward A.; Strieder, John W.

doi:10.1016/0002-9343(53)90282-4

Cited by 7 publications

(7 citation statements)

References 0 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…A syndrome in which one lung is more transradiant than the other has been recognized increasingly since the original reports by Madoff, Gaensler, and Strieder (1952), Swyer and James (1953), and Macleod (1954). Macleod described the following features: lessening of the radiographic markings with persistently greater transradiancy over one lung; and quietening of the breath sounds in the same lung.…”

mentioning

confidence: 99%

Cardiopulmonary performance at rest and during exercise in seven patients with increased transradiancy of one lung (`Macleod's syndrome')

Warrell

Hughes

Rosenzweig

1970

Thorax

View full text Add to dashboard Cite

mentioning

confidence: 99%

Cardiopulmonary performance at rest and during exercise in seven patients with increased transradiancy of one lung (`Macleod's syndrome')

Warrell

Hughes

Rosenzweig

1970

Thorax

View full text Add to dashboard Cite

“…UAPA was first described in 1868 by Frantzel O. Angeborener, and later it was proven angiographically by Madoff and his colleagues in 1953 [4]. It has been estimated that the prevalence of this unique disorder is about one in 200,000 [5].…”

Section: Discussionmentioning

confidence: 99%

A Rare Case of Isolated Unilateral Atresia of Pulmonary Artery in an Elderly Female

Ain

Khan

Sherazi

et al. 2019

Cureus

View full text Add to dashboard Cite

Isolated unilateral agenesis/atresia of pulmonary artery (IUAPA) is a rare congenital disorder, an uncommon variant of unilateral agenesis of pulmonary artery (UAPA). Patients with IUAPA may remain asymptomatic and undiagnosed till late adulthood as they present with vague symptoms which may be overlooked. We report a case of IUAPA of right pulmonary artery in an elderly female who presented with complaints of productive cough and exertional dyspnea. Due to the formation of extensive collaterals, her lung parenchyma was preserved.

show abstract

“…The exact prevalence is unknown; however, the estimated prevalence is 1 in every 200,000 individuals . The first report of a surgical repair for UAPPA was by Madoff et al in 1952 …”

Section: Discussionmentioning

confidence: 99%

Surgical repair of a truncus arteriosus with unilateral absence of the right proximal pulmonary artery

et al. 2016

View full text Add to dashboard Cite

The unilateral absence of a proximal pulmonary artery (UAPPA) is rare and is most frequently accompanied by cardiovascular anomalies such as tetralogy of Fallot or septal defects. We report a patient with truncus arteriosus with UAPPA in which we performed a two-stage surgical repair. During the first palliative operation, a right modified Blalock-Taussig shunt was constructed to develop the hypoplastic right pulmonary artery. At 10 months, the patient underwent patch closure of a ventricular septal defect with integration of both pulmonary arteries, and reconstruction of the right ventricular outflow tract using a conduit. Four years postoperatively, he continues to do well.

show abstract

Congenital absence of the right pulmonary artery diagnosed by angiocardiography and cardiorespiratory studies

Cited by 7 publications

References 0 publications

Cardiopulmonary performance at rest and during exercise in seven patients with increased transradiancy of one lung (`Macleod's syndrome')

Cardiopulmonary performance at rest and during exercise in seven patients with increased transradiancy of one lung (`Macleod's syndrome')

A Rare Case of Isolated Unilateral Atresia of Pulmonary Artery in an Elderly Female

Surgical repair of a truncus arteriosus with unilateral absence of the right proximal pulmonary artery

Contact Info

Product

Resources

About