Concurrent Morgagni and Bochdalek congenital diaphragmatic hernias with omphalocele
| Autor: | Kelly Austin, Burhan Mahmood, Abeer Azzuqa, Bryanna Emr, Ayesha M. Sulaiman, Insiyah Campwala |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Thorax
medicine.medical_specialty RD1-811 Diaphragmatic breathing Congenital diaphragmatic hernia Bochdalek hernia Pediatrics RJ1-570 Abdominal wall 03 medical and health sciences Pulmonary hypoplasia 0302 clinical medicine Morgagni hernia Medicine Craniofacial Omphalocele business.industry medicine.disease digestive system diseases Surgery Diaphragm (structural system) stomatognathic diseases medicine.anatomical_structure surgical procedures operative 030220 oncology & carcinogenesis Pediatrics Perinatology and Child Health 030211 gastroenterology & hepatology business |
| Zdroj: | Journal of Pediatric Surgery Case Reports, Vol 70, Iss, Pp 101890-(2021) |
| ISSN: | 2213-5766 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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