Right-sided bochdalek hernia associated with esophageal atresia and tracheo-esophageal fistula

Ahmed, Saeed

doi:10.1016/0022-3468(70)90284-8

Cited by 14 publications

(5 citation statements)

References 1 publication

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“…Other malformations included lung agenesis (18.5%), Meckel's diverticulum (14.8%), renal dysplasia (11.1%), trisomy 18 (7.4%), spinal deformities (7.4%), and facial deformities (3.7%). CDH, EA, and TEF are fatal deformities in children; however, surgery has been the key to saving their lives since 1970 ( 4 ).…”

Section: Discussionmentioning

confidence: 99%

Case Report: Congenital diaphragmatic hernia associated with esophageal atresia and tracheoesophageal fistula

Zhang

Wu²,

Zhang³

et al. 2023

Front. Surg.

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Section: Discussionmentioning

confidence: 99%

Case Report: Congenital diaphragmatic hernia associated with esophageal atresia and tracheoesophageal fistula

Zhang

Wu²,

Zhang³

et al. 2023

Front. Surg.

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“…The combination of CDH and OA is so rare that the association is seldom suspected. Prompt recognition of a TOF in the presence of CDH is essential to prevent life-threatening respiratory compromise by progressive gaseous distension of the herniated bowel during positive pressure ventilation (Ahmed 1970;Bowen 1983;Rawlings et al 1984) but not in the absence of a TOF when no air will enter the gastrointestinal tract (Udassin et al 1987). The problem is exacerbated by poorly compliant lungs.…”

Section: Discussionmentioning

confidence: 99%

“…Eighteen cases have been reported in the English literature ( Table 1). The combination poses significant management problems (Ahmed 1970;Bowen 1983). In the presence of TOF, clearly positive pressure ventilation will provoke gastric distension with deterioration of gas exchange, especially if the stomach lies within the chest.…”

Section: Introductionmentioning

confidence: 99%

Management of oesophageal atresia in association with congenital diaphragmatic hernia

Bösenberg

Mickel

Hadley

1994

Pediatric Anesthesia

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Summa yOesophageal atresia (OA) with or without a tracheo-oesophageal fistula (TOF) is rarely associated with congenital diaphragmatic hernia (CDH). The combination poses significant management problems and the mortality rate is high. Two patients with CDH and associated OA are presented and their management outlined. Early recognition of the TOF is essential to prevent increasing respiratory compromise by gaseous distension of herniated bowel within the thorax. A staged surgical approach involving initial repair of the CDH allowing left lung function to improve prior to right thoracotomy and ligation of the TOF with oesophageal anastomosis may improve outcome. The presence of other life-threatening anomalies and/or chromosomal abnormalities must be evaluated prior to embarking upon definitive treatment.

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“…Until 2015 there were only two database publications in relevant literature, announced in 2005 and 2013, and each reports approximately 20 cases of CDH with EA from different registries 1, 2 . Only 13 cases were reported in details [2][3][4][5][6][7][8][9][10][11] , and all cases were sporadic, presented as case reports. Of those 13, there were only 3 case reports with successful management and survival of an infant with left CDH, EA, and TEF [3][4][5] .…”

Section: Congenitalmentioning

confidence: 99%

Congenital diaphragmatic hernia associated with esophageal atresia, tracheoesophageal fistula and total anomalous pulmonary venous connection in a premature twin newborn

et al. 2019

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Introduction. Congenital diaphragmatic hernia (CDH) with concomitant esophageal atresia (EA) and tracheo-esophageal fistula (TEF) is a very rare condition, with a high mortality rate. Prematurity and congenital heart anomalies additionally increase the mortality rate. This situation is a great challenge for clinicians, requiring multidisciplinary work and adequate treatment strategy. Case report. We presented a premature twin newborn at the gestational age of 33/34 weeks with body mass of 1690 g. The existence of the left CDH was established on prenatal ultrasound exam in the 24th gestational week, and the diagnosis of EA with TEF was made on admittance to our hospital. The cardiac ultrasound exam revealed the total anomalous pulmonary venous connection (TAPVC). The first operation was performed on the day of admittance and consisted of left subcostal laparotomy, diaphragmatic repair, elastic occlusion of the gastroesophageal junction and gastrostomy. The ligation

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Right-sided bochdalek hernia associated with esophageal atresia and tracheo-esophageal fistula

Cited by 14 publications

References 1 publication

Case Report: Congenital diaphragmatic hernia associated with esophageal atresia and tracheoesophageal fistula

Case Report: Congenital diaphragmatic hernia associated with esophageal atresia and tracheoesophageal fistula

Management of oesophageal atresia in association with congenital diaphragmatic hernia

Congenital diaphragmatic hernia associated with esophageal atresia, tracheoesophageal fistula and total anomalous pulmonary venous connection in a premature twin newborn

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