Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report

Incidence of congenital cystic malformation of lungs ranges from 1 in 11,000 to 1 in 35,000 live birth. Concurrence of Congenital Pulmonary Airway Malformation (CPAM) with congenital heart disease is even infrequent. Even rarer, is the incidence of congenital pulmonary vascular and cystic parenchy...

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Main Authors: Lakshmi Sinha, Debmalya Saha, Sayyed Ehtesham Hussain Naqvi, Muhammad Abid Geelani, Vishnu Datt
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2022-10-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/16921/56689_CE(AnK)_F(KM)_PF1(SC_SS)_PFA(SS)_PB(SC_SS)_PN(SS).pdf
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author Lakshmi Sinha
Debmalya Saha
Sayyed Ehtesham Hussain Naqvi
Muhammad Abid Geelani
Vishnu Datt
author_facet Lakshmi Sinha
Debmalya Saha
Sayyed Ehtesham Hussain Naqvi
Muhammad Abid Geelani
Vishnu Datt
author_sort Lakshmi Sinha
collection DOAJ
description Incidence of congenital cystic malformation of lungs ranges from 1 in 11,000 to 1 in 35,000 live birth. Concurrence of Congenital Pulmonary Airway Malformation (CPAM) with congenital heart disease is even infrequent. Even rarer, is the incidence of congenital pulmonary vascular and cystic parenchymal lesions with cardiac defects. The non functioning lung tissue is separated from bronchial tree and vascularised by aberrant artery from the systemic circulation. Simultaneous repair of cardiac and pulmonary defects, though challenging, but are preferable because of surgery being done in single stage with better cosmesis. A 10-yearold female child presented to the hospital with recurrent chest infections and respiratory distress while running since five years of age. The patient underwent atrial septal defect closure and right lower lobectomy for CPAM in one stage through midline sternotomy. We conclude that such complex cases can be managed successfully with meticulous planning and multidisciplinary team approach.
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spelling doaj.art-bfaab1ad1dd9435ea3e43e64d4abd0832023-02-24T05:59:23ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2022-10-011610PD04PD0610.7860/JCDR/2022/56689.16921Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case ReportLakshmi Sinha0Debmalya Saha1Sayyed Ehtesham Hussain Naqvi2Muhammad Abid Geelani3Vishnu Datt4Resident, Department of Cardiothoracic Vascular Surgery, Govind Ballabh Pant Hospital, New Delhi, India.Resident, Department of Cardiothoracic Vascular Surgery, Govind Ballabh Pant Hospital New Delhi, India.Associate Professor, Department of Cardiothoracic Vascular Surgery, Govind Ballabh Pant Hospital, New Delhi, India.Professor, Director and Head, Department of Cardiothoracic Vascular Surgery, Govind Ballabh Pant Hospital, New Delhi, India.Professor, Director and Head Department of Anaesthesiology, Govind Ballabh Pant Hospital, New Delhi, India.Incidence of congenital cystic malformation of lungs ranges from 1 in 11,000 to 1 in 35,000 live birth. Concurrence of Congenital Pulmonary Airway Malformation (CPAM) with congenital heart disease is even infrequent. Even rarer, is the incidence of congenital pulmonary vascular and cystic parenchymal lesions with cardiac defects. The non functioning lung tissue is separated from bronchial tree and vascularised by aberrant artery from the systemic circulation. Simultaneous repair of cardiac and pulmonary defects, though challenging, but are preferable because of surgery being done in single stage with better cosmesis. A 10-yearold female child presented to the hospital with recurrent chest infections and respiratory distress while running since five years of age. The patient underwent atrial septal defect closure and right lower lobectomy for CPAM in one stage through midline sternotomy. We conclude that such complex cases can be managed successfully with meticulous planning and multidisciplinary team approach.https://jcdr.net/articles/PDF/16921/56689_CE(AnK)_F(KM)_PF1(SC_SS)_PFA(SS)_PB(SC_SS)_PN(SS).pdfcongenital pulmonary airway malformationcongenital heart diseasecongenital cystic adenomatoid malformationright lower lobectomy
spellingShingle Lakshmi Sinha
Debmalya Saha
Sayyed Ehtesham Hussain Naqvi
Muhammad Abid Geelani
Vishnu Datt
Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
Journal of Clinical and Diagnostic Research
congenital pulmonary airway malformation
congenital heart disease
congenital cystic adenomatoid malformation
right lower lobectomy
title Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
title_full Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
title_fullStr Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
title_full_unstemmed Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
title_short Surgical Repair of Atrial Septal Defect and Lung Lobe Resection for Pulmonary Sequestration and Cystic Malformation in One Stage: A Case Report
title_sort surgical repair of atrial septal defect and lung lobe resection for pulmonary sequestration and cystic malformation in one stage a case report
topic congenital pulmonary airway malformation
congenital heart disease
congenital cystic adenomatoid malformation
right lower lobectomy
url https://jcdr.net/articles/PDF/16921/56689_CE(AnK)_F(KM)_PF1(SC_SS)_PFA(SS)_PB(SC_SS)_PN(SS).pdf
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