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Unilateral pulmonary aplasia and congenital diaphragmatic hernia associated with tetralogy of Fallot: a rare trifecta

Published online by Cambridge University Press:  09 January 2020

Niraj N. Pandey Open the ORCID record for Niraj N. Pandey [Opens in a new window] ,
Mumun Sinha  and
Sanjeev Kumar
Niraj N. Pandey
Affiliation:
Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India
Mumun Sinha
Affiliation:
Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India
Sanjeev Kumar*
Affiliation:
Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India
*
Author for Correspondence: Dr S. Kumar, Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi 110029, India. Tel.: +91-9968968918; E-mail: [email protected]
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Abstract

We present a case of a 7-month-old boy with tetralogy of Fallot associated with unilateral pulmonary aplasia and herniation of the liver and small bowel loops in the right hemithorax.

Keywords

Tetralogy of Fallotpulmonary aplasiacongenital diaphragmatic hernia
Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 30 , Issue 1 , January 2020 , pp. 121 - 122
Copyright
© Cambridge University Press 2020

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References

Boyden, EA.Developmental anomalies of the lungs. Am J Surg 1955; 89: 79–89.CrossRefGoogle ScholarPubMed
Labovsky, K, Hoffman, G, Scott, J.Management of a patient with tetralogy of Fallot, congenital diaphragmatic hernia, and complete left lung agenesis. A A Case Rep 2016; 7: 16–20.CrossRefGoogle ScholarPubMed