Results 11 to 20 of about 35,475 (152)

Jejunal atresia associated with jejunal diverticulosis

open access: yesJournal of Pediatric Surgery Case Reports, 2018
Jejunoilial atresia is a frequent cause of bowel obstruction in neonates, with prevalence around 0.7 per 10000 livebirths. It is believed to be related to an intrauterine vascular accident that commonly presents as isolated pathology.
Hamdi H. Almaramhy
doaj   +2 more sources

The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn

open access: yesCase Reports in Pediatrics, 2015
We encountered a rare case of gastroschisis associated with jejunal atresia and colonic atresia. In our case, the jejunal atresia was not discovered for 27 days after the initial abdominal wall closure.
Zachary Bauman, Victor Nanagas
doaj   +3 more sources

Duodeno-jejunal Atresia with Apple-peel Appearance of the Remaining Ileum: A Rare Association

open access: yesMAMC Journal of Medical Sciences, 2015
Intestinal atresia is a common cause of neonatal intestinal obstruction. We present a rare case of duodenal atresia, multiple jejunal atresias, and apple peel appearance of the remaining ileum in a 3-day-old neonate.
Abhishek Chinya   +2 more
doaj   +2 more sources

Jejunal atresia associated with idiopathic ileal perforation [PDF]

open access: yesJournal of Indian Association of Pediatric Surgeons, 2008
Jejunoileal atresia is one of the common causes of neonatal intestinal obstruction. Intestinal perforation with meconium peritonitis in the neonatal period, which carries a high mortality rate, is also common.
Das P, Rai Rakesh, Lobo Grover
doaj   +4 more sources

002. Case Report: High Jejunal Atresia Type 1 Treated by Side to Side Anastomosis Jejuno-Jejunostomy [PDF]

open access: yesJBN (Jurnal Bedah Nasional)
Background: Jejunal atresia characterized by complete occlusion lumen of the intestinal, is a rare congenital abnormality occurring in 1 out of 12.000 live births.
Wildan Kharisma Zisnanda   +3 more
doaj   +2 more sources

Apple peel jejunal atresia: Successful management of a rare case

open access: yesJournal of the Scientific Society, 2012
Apple peel jejunal atresia is a rare congenital anomaly. This condition presents at birth as an intestinal obstruction, is diagnosed by X-rays and confirmed by laparatomy.
Santosh B Kurbet   +4 more
doaj   +2 more sources

Duodenal Derotation and Extent Tapering Jejunoplasty as Primary Repair for Neonates With High Jejunal Atresia [PDF]

open access: yesPediatrics and Neonatology, 2010
The dilated bowel segment usually involves the entire jejunum, as well as the duodenum in patients with high jejunal atresia. Classical approaches with a limited tapering enteroplasty and anastomosis frequently fail to restore intestinal function.
Chih-Cheng Luo   +3 more
doaj   +2 more sources

Heterotopic gastric mucosa associated with jejunal atresia

open access: yesJournal of Pediatric Surgery Case Reports, 2019
An infant born at 35 weeks' gestation with type 2 jejunal atresia underwent resection of the atretic ends of the bowel and primary anastomosis. Histologic examination of the resected distal bowel segment revealed heterotopic gastric mucosa (HGM).
Olivia M. Parker   +2 more
doaj   +2 more sources

Jejunal atresia causing failure to thrive: The role of camera mobile phones in aiding diagnosis in limited resource settings

open access: yesJournal of Pediatric Surgery Case Reports, 2018
Type 1 jejunal atresias with partial webs present with intermittent features of high grade, partial intestinal obstruction potentially delaying diagnosis, particularly in low resource countries with limited access to advanced imaging technology.
Paddy Ssentongo   +7 more
doaj   +2 more sources

Missed proximal jejunal web during repair of jejunal atresia: a case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Jejunoileal atresia repair commonly involves interrogation of the bowel distal for additional atresias, although rare, the practice of proximal bowel interrogation for an additional proximal atresia should be considered.
Sara L. Lee   +2 more
doaj   +2 more sources

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