{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,7]],"date-time":"2026-03-07T10:52:27Z","timestamp":1772880747223,"version":"3.50.1"},"reference-count":10,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2017,7,31]]},"abstract":"<jats:p>We reported a rare case of left-sided posterolateral congenital diaphragmatic hernia (CDH) and omphalocele, which is not associated with chromosomal abnormalities or other syndromes. Omphalocele was detected antenatally (CDH was not detected in antenatal ultrasound). The patient suffered from respiratory failure secondary to severe pulmonary hypertension. As the combination of CDH and omphalocele is rare and with the abdominal content herniating into the omphalocele instead of the thorax, antenatal diagnosis of such condition can be difficult. Unlike other reported cases in the literature, our patient's respiratory condition has been improving with time and is surviving beyond the infancy period. We believe this to be the first such survival case reported in the literature.<\/jats:p>","DOI":"10.1136\/bcr-2017-220696","type":"journal-article","created":{"date-parts":[[2017,8,8]],"date-time":"2017-08-08T10:11:58Z","timestamp":1502187118000},"page":"bcr-2017-220696","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":6,"title":["Rare combination of left-sided congenital diaphragmatic hernia and omphalocele"],"prefix":"10.1136","volume":"2017","author":[{"given":"Yuet Yee","family":"Chee","sequence":"first","affiliation":[{"name":"Department of Paediatrics and Adolescent Medicine, University of Hong Kong, Hong Kong, Hong Kong"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Siu Chun Mabel","family":"Wong","sequence":"additional","affiliation":[{"name":"Department of Paediatrics and Adolescent Medicine, University of Hong Kong, Hong Kong, Hong Kong"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ming Sum Rosanna","family":"Wong","sequence":"additional","affiliation":[{"name":"Department of Paediatrics and Adolescent Medicine, University of Hong Kong, Hong Kong, Hong Kong"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2017,8,7]]},"reference":[{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.1","first-page":"331","article-title":"Associated malformations in cases with congenital diaphragmatic hernia","volume":"19","author":"Stoll","year":"2008","journal-title":"Genet Couns"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.2","doi-asserted-by":"crossref","first-page":"1280","DOI":"10.1002\/ajmg.a.32297","article-title":"Omphalocele and gastroschisis and associated malformations","volume":"146A","author":"Stoll","year":"2008","journal-title":"Am J Med Genet A"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.3","doi-asserted-by":"crossref","first-page":"2298","DOI":"10.1002\/ajmg.a.31470","article-title":"Associated malformations in congenital diaphragmatic hernia cases in the last 15 years in a tertiary referral institute","volume":"140","author":"Harmath","year":"2006","journal-title":"Am J Med Genet A"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.4","doi-asserted-by":"publisher","DOI":"10.1136\/adc.69.1_Spec_No.68"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.5","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1007\/s10024-003-2133-7","article-title":"Congenital diaphragmatic hernia and chromosomal anomalies: autopsy study","volume":"7","author":"Borys","year":"2004","journal-title":"Pediatr Dev Pathol"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.6","doi-asserted-by":"publisher","DOI":"10.1086\/513442"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.7","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1186\/s13256-016-0805-y","article-title":"Coexistence of congenital diaphragmatic hernia and abdominal wall closure defect with chromosomal abnormality: two case reports","volume":"10","author":"Inoue","year":"2016","journal-title":"J Med Case Rep"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.8","doi-asserted-by":"publisher","DOI":"10.1378\/chest.101.1.263"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.9","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1002\/ajmg.a.35703","article-title":"Anterolateral congenital diaphragmatic hernia with omphalocele: a case report and literature review","volume":"161A","author":"Scahill","year":"2013","journal-title":"Am J Med Genet A"},{"key":"2025082703380965000_2017.aug07_2.bcr-2017-220696.10","doi-asserted-by":"crossref","first-page":"n\/a","DOI":"10.1111\/cga.12075","article-title":"Prenatal imaging of a fetus with the rare combination of a right congenital diaphragmatic hernia and a giant omphalocele","volume":"54","author":"Nonaka","year":"2014","journal-title":"Congenit Anom"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2017-220696","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,27]],"date-time":"2025-08-27T10:38:19Z","timestamp":1756291099000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2017-220696"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,8,7]]},"references-count":10,"alternative-id":["10.1136\/bcr-2017-220696"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2017-220696","relation":{},"ISSN":["1757-790X"],"issn-type":[{"value":"1757-790X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,8,7]]}}}