scholarly journals Anomalous pancreatic ductal system allowing distal bowel gas with duodenal atresia

2017 ◽  
Vol 26 ◽  
pp. 7-10 ◽  
Author(s):  
Shruti Sevak ◽  
Begum Akay ◽  
David A. Bloom
2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Surasak Puvabanditsin ◽  
Marissa Botwinick ◽  
Charlotte Wang Chen ◽  
Aditya Joshi ◽  
Rajeev Mehta

Background. The presence of distal bowel gas in an infant does not exclude the diagnosis of duodenal atresia. Case Presentation. We report a term neonate with Down syndrome. The infant developed vomiting and cyanosis with each feeding soon after birth. Plain film abdominal X-rays showed a nonspecific gas-filled stomach and small bowel. Duodenal atresia and an anomalous common bile were noted on an upper GI study and exploratory laparotomy. Conclusion. In the absence of a “double bubble” appearance and intestinal gas distally on a plain radiograph, one must not exclude duodenal atresia as the differential diagnosis.


Author(s):  
Maria Enrica Miscia ◽  
Giuseppe Lauriti ◽  
Dacia Di Renzo ◽  
Angela Riccio ◽  
Gabriele Lisi ◽  
...  

Abstract Introduction Esophageal atresia (EA) is associated with duodenal atresia (DA) in 3 to 6% of cases. The management of this association is controversial and literature is scarce on the topic. Materials and Methods We aimed to (1) review the patients with EA + DA treated at our institution and (2) systematically review the English literature, including case series of three or more patients. Results Cohort study: Five of seventy-four patients with EA had an associated DA (6.8%). Four of five cases (80%) underwent primary repair of both atresia, one of them with gastrostomy placement (25%). One of five cases (20%) had a delayed diagnosis of DA. No mortality has occurred. Systematic Review: Six of six-hundred forty-five abstract screened were included (78 patients). Twenty-four of sixty-eight (35.3%) underwent primary correction of EA + DA, and 36/68 (52.9%) underwent staged correction. Nine of thirty-six (25%) had a missed diagnosis of DA. Thirty-six of sixty-eight underwent gastrostomy placement. Complications were observed in 14/36 patients (38.9 ± 8.2%). Overall mortality reported was 41.0 ± 30.1% (32/78 patients), in particular its incidence was 41.7 ± 27.0% after a primary treatment and 37.0 ± 44.1% following a staged approach. Conclusion The management of associated EA and DA remains controversial. It seems that the staged or primary correction does not affect the mortality. Surgeons should not overlook DA when correcting an EA.


1997 ◽  
Vol 32 (12) ◽  
pp. 1806-1808 ◽  
Author(s):  
Takahide Yokoyama ◽  
Shinpachi Ishizone ◽  
Yoshitaka Momose ◽  
Masaru Terada ◽  
Shuuichirou Kitahara ◽  
...  

2019 ◽  
Vol 12 (8) ◽  
pp. e230160
Author(s):  
Jyotsna M Kirtane ◽  
Snehal A Bhange ◽  
Fazal Nabi ◽  
Varshil Shah

This is a case report of a neonate who was antenatally diagnosed with jejunal atresia which turned out to be duodenal atresia with apple peel syndrome. A previous sibling, who also had apple peel but with jejunal atresia, succumbed to sepsis after surgery. The first sibling had jejunal stenosis and had died of sepsis following surgery. Combination of duodenal atresia with apple peel is extremely rare. This coupled with a familial condition is rarer still. This case was challenging due to the short length of the gut and prolonged need for total parenteral nutrition and sepsis in postoperative period.


2014 ◽  
Vol 44 (8) ◽  
pp. 1031-1034 ◽  
Author(s):  
Jonathan M. Latzman ◽  
Terry L. Levin ◽  
Suhas M. Nafday

2007 ◽  
Vol 27 (4) ◽  
pp. 381-383 ◽  
Author(s):  
Jeng-Hsiu Hung ◽  
Shu-Huei Shen ◽  
Tai-Wai Chin ◽  
Chia-Yi Selena Hung

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