Hybrid Pulmonary Sequestration, Cystic Pulmonary Adenomatoid Malformation, and Dextrocardia: A Triple Whammy

Author:

Bajpai Jyoti1,Verma Shreya2,Kant Surya1,Verma Ajay Kumar1,Bajaj Darshan1,Pradhan Akshyaya3,Bhalla Shalini4

Affiliation:

1. Department of Respiratory Medicine, King George’s Medical University, Lucknow, Uttar Pradesh, India

2. Department of Faculty of Medical Sciences, King George’s Medical University, Lucknow, Uttar Pradesh, India

3. Department of Cardiology, King George’s Medical University, Lucknow, Uttar Pradesh, India

4. Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India

Abstract

Abstract Pulmonary sequestration and cystic pulmonary adenomatoid malformation are rare congenital cystic disorders of the lungs. The presence of both the diseases in the same individual is therefore very uncommon. Pulmonary sequestration is a nonfunctional pulmonary tissue mass that derives its blood supply from systemic blood supply other than pulmonary circulation. Congenital cystic pulmonary adenomatoid malformation represents a mass consisting of abnormal bronchiolar air spaces and a deficiency of functional alveoli. This is the case report of a 9-year-old girl with intermittent fever, left-sided chest pain, and cough for the past 15 days along with recurrent coughs since childhood suggestive of hybrid pulmonary sequestration, congenital cystic adenomatoid malformation, and dextrocardia.

Publisher

Medknow

Reference12 articles.

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