Results 1 to 10 of about 1,117 (123)

Persistent Ompahalomesenteric Duct in a Newborn With 16p11.2 Deletion: Report of New Findings [PDF]

Clinical Case Reports
Omphalomesenteric duct (OMD) is an embryologic communication between the extraembryonic yolk sac and the primitive midgut. The OMD malformations are relatively rare diseases associated with developmental defects related to the closure of the ...
Surasak Puvabanditsin, Sathyaprasad Burjonrappa, Natasha Cordero, Su Young Park, Jenny Choi, Amrryn Halari, Dawn Arumemi, Rajeev Mehta   +7 more
doaj   +3 more sources

Omphalomesenteric duct remnant: A rare and unusual cause of intestinal atresia [PDF]

Journal of Indian Association of Pediatric Surgeons, 2021
Intestinal atresia is generally considered to result from mesenteric vascular disruptions during fetal life. This report describes an unusual case of ileal atresia, resulting from an omphalic ring closure anomaly and an omphalomesenteric duct (OMD ...
Gavin Kane, Hind Zaidan, Brice Antao
doaj   +2 more sources

Double ileoileal intussusception prolapse through persistent omphalomesenteric duct

Journal of Pediatric Surgery Case Reports, 2021
Double prolapsed intussusception is a rare complication of persistent omphalomesenteric duct and it represents a surgical emergency. Any delay in its management may lead to a negative outcome.
Martial Olivier Moulot, Tudor Enache, Kouamé Agbara, Manuela Ehua, Guy Serge Kouame Yapo, Sekinatou Oyewola, Helen Audrey Thomas, Jean - Marie Konan, Roumanatou Bankolé S   +8 more
exaly   +3 more sources

Omphalocele with intestinal prolapse through a patent omphalomesenteric duct: A case report

Journal of Pediatric Surgery Case Reports, 2023
Introduction: The combination of a patent omphalomesenteric duct in the setting of an omphalocele is rare and has an unusual physical appearance on presentation.
Kulaylat An, Aodhnait S Fahy
exaly   +3 more sources

Omphalomesenteric duct & Urachal remnant presentation in a newborn

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Persistent urachal anomalies are rare congenital pathologies caused by a failure of obliteration of the urachal remnant, whereas a patent omphalomesenteric duct is due to an incomplete obliteration of the vitelline duct.
Sarah Ellul
exaly   +3 more sources

Unusual Ileal Anomalies Associated with Omphalomesenteric Duct Remnants

African Journal of Paediatric Surgery, 2017
The association between omphalomesenteric duct remnants and other digestive tract malformations is not rare. Most associated anomalies are reported with Meckel's diverticulum.
Mohamed Ouladsaiad, Najoua Aballa, El Ouafi El Aouni Kamili, Karima Fouraiji   +3 more
doaj   +2 more sources

Heterotopic pancreas in the omphalomesenteric duct remnant in a 9-month-old girl: a case report and literature review [PDF]

Diagnostic Pathology, 2017
Background Heterotopic pancreas most commonly occurs in the upper gastrointestinal tract of adults, usually as an incidental finding. It seldom occurs at the umbilicus, and even rarely in the pediatric age group.
Zitong Zhao, Chiang Khi Sim, Sangeeta Mantoo   +2 more
doaj   +2 more sources

Persistent Umbilical Discharge from an Omphalomesenteric Duct Cyst Containing Gastric Mucosa [PDF]

Case Reports in Pediatrics, 2012
Umbilical discharge in infancy is often attributed to infection or an umbilical granuloma. It is important to investigate if such a discharge is due to an underlying congenital abnormality because corrective surgical intervention may then be required. We
Kanimozhi Tamilselvan, Arunodaya Mohan, Sarah Cheslyn-Curtis, Michael Eisenhut   +3 more
doaj   +2 more sources

Ileal prolapse through patent omphalomesenteric duct in a two year-old boy: a case report [PDF]

Journal of Medical Case Reports
Background Patent omphalomesenteric duct is one of the birth defects included in the spectrum of vitelline duct abnormalities. It is a rare anomaly with estimated prevalence of 0.13–0.2% in the general population.
Binyam Yohannes Wolde Hawariat, Amal Ousman Ali, Hana Abebe Gebreselassie   +2 more
doaj   +2 more sources

Axial Torsion of a Necrotic Giant Meckel's Diverticulum With Secondary Peritonitis in a 7-Year-Old: A Case Report. [PDF]

Case Rep Surg
Axial torsion with subsequent gangrene of Meckel’s diverticulum represents an exceptionally rare cause of small bowel obstruction, one of the rarest causes of small bowel obstruction. Meckel’s diverticulum is the most common congenital anomaly of the gastrointestinal tract, and it is often discovered incidentally during abdominal surgery, particularly ...
Trăilescu MD, Pavel AI, Crișan AS, Cindea CN, Osakwe HI, Boștinaru GM.   +5 more
europepmc   +2 more sources