Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele
Congenital diaphragmatic hernia (CDH) is a well-documented developmental abnormality in the formation of the diaphragm, resulting in herniation of bowel into the thorax causing pulmonary hypoplasia. CDH has been associated with many genetic syndromes and other anatomic anomalies including craniofaci...
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| Format: | Article |
| Language: | English |
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Elsevier
2021-07-01
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| Series: | Journal of Pediatric Surgery Case Reports |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2213576621001111 |
| _version_ | 1818597530906132480 |
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| author | Insiyah Campwala Bryanna Emr Ayesha M. Sulaiman Abeer A. Azzuqa Burhan Mahmood Kelly Austin |
| author_facet | Insiyah Campwala Bryanna Emr Ayesha M. Sulaiman Abeer A. Azzuqa Burhan Mahmood Kelly Austin |
| author_sort | Insiyah Campwala |
| collection | DOAJ |
| description | Congenital diaphragmatic hernia (CDH) is a well-documented developmental abnormality in the formation of the diaphragm, resulting in herniation of bowel into the thorax causing pulmonary hypoplasia. CDH has been associated with many genetic syndromes and other anatomic anomalies including craniofacial, cardiac, skeletal, brain, ocular, renal, and abdominal wall defects. Despite this, co-occurrence of CDH and omphalocele is rare and only identified within 0.63% of neonates with CDH. Most congenital diaphragmatic hernias are located posterolateral (Bochdalek hernias) or anterior retrosternal or parasternal (Morgagni hernias); bilateral diaphragmatic hernias are rare. We describe the first documented case of concurrent Bochdalek and Morgagni hernias with an omphalocele and no other associated anatomic anomalies. |
| first_indexed | 2024-12-16T11:49:17Z |
| format | Article |
| id | doaj.art-b4b44d376f1d419aae2cb58125c0fcb7 |
| institution | Directory Open Access Journal |
| issn | 2213-5766 |
| language | English |
| last_indexed | 2024-12-16T11:49:17Z |
| publishDate | 2021-07-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Journal of Pediatric Surgery Case Reports |
| spelling | doaj.art-b4b44d376f1d419aae2cb58125c0fcb72022-12-21T22:32:45ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662021-07-0170101890Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphaloceleInsiyah Campwala0Bryanna Emr1Ayesha M. Sulaiman2Abeer A. Azzuqa3Burhan Mahmood4Kelly Austin5Division of Pediatric General and Thoracic Surgery, Department of Surgery, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USADivision of Pediatric General and Thoracic Surgery, Department of Surgery, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USADivision of Newborn Medicine, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USADivision of Newborn Medicine, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USADivision of Newborn Medicine, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USADivision of Pediatric General and Thoracic Surgery, Department of Surgery, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Corresponding author. One Children's Hospital Drive, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.Congenital diaphragmatic hernia (CDH) is a well-documented developmental abnormality in the formation of the diaphragm, resulting in herniation of bowel into the thorax causing pulmonary hypoplasia. CDH has been associated with many genetic syndromes and other anatomic anomalies including craniofacial, cardiac, skeletal, brain, ocular, renal, and abdominal wall defects. Despite this, co-occurrence of CDH and omphalocele is rare and only identified within 0.63% of neonates with CDH. Most congenital diaphragmatic hernias are located posterolateral (Bochdalek hernias) or anterior retrosternal or parasternal (Morgagni hernias); bilateral diaphragmatic hernias are rare. We describe the first documented case of concurrent Bochdalek and Morgagni hernias with an omphalocele and no other associated anatomic anomalies.http://www.sciencedirect.com/science/article/pii/S2213576621001111Congenital diaphragmatic herniaBochdalek herniaMorgagni herniaOmphalocele |
| spellingShingle | Insiyah Campwala Bryanna Emr Ayesha M. Sulaiman Abeer A. Azzuqa Burhan Mahmood Kelly Austin Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele Journal of Pediatric Surgery Case Reports Congenital diaphragmatic hernia Bochdalek hernia Morgagni hernia Omphalocele |
| title | Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele |
| title_full | Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele |
| title_fullStr | Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele |
| title_full_unstemmed | Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele |
| title_short | Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele |
| title_sort | concurrent morgagni and bochdalek congenital diaphragmatic hernias with omphalocele |
| topic | Congenital diaphragmatic hernia Bochdalek hernia Morgagni hernia Omphalocele |
| url | http://www.sciencedirect.com/science/article/pii/S2213576621001111 |
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