Results 61 to 70 of about 611,084 (238)

Waugh's Syndrome: Report of Two Children with Intussusception

open access: yesEuropean Journal of Pediatric Surgery Reports, 2017
Waugh's syndrome (WS) is the rare association of intussusception and intestinal malrotation. We present two such cases in a 5-month-old infant and a 9-year-old girl.
Yousuf Aziz Khan   +2 more
doaj   +1 more source

Preduodenal Portal Vein Associated With Intestinal Malrotation and Jejunal Atresia

open access: yesCureus, 2021
Preduodenal portal vein (PDPV) is a rare congenital anomaly commonly associated with other gastrointestinal abnormalities. We report the case of a female neonate with a PDPV, intestinal malrotation and jejunal atresia.
David Zula   +3 more
semanticscholar   +1 more source

Duodenal duplication, intestinal malrotation and volvulus: An unusual cause of intestinal obstruction

open access: yesJournal of Pediatric Surgery Case Reports, 2016
Duodenal duplication cysts are unusual congenital anomalies. Both intestinal malrotation and duodenal duplication may cause extrinsic duodenal obstruction.
Ivonete Siviero   +4 more
doaj   +1 more source

Fetal malrotation with midgut volvulus: Prenatal diagnosis and planning

open access: yesJournal of Pediatric Surgery Case Reports, 2023
Introduction: Malrotation of the intestinal tract is a congenital malformation commonly found either incidentally or after affected individuals develop signs and symptoms of intestinal obstruction.
Oluyinka O. Olutoye II   +12 more
doaj   +1 more source

Intestinal malrotation and Meckel’s diverticulitis in a 19-month-old boy

open access: yesBJR|case reports, 2021
Acute intestinal obstruction is a common paediatric surgical emergency and should be considered in any child presenting with vomiting, abdominal pain and abdominal distension.
Nida Mushtaq   +5 more
semanticscholar   +1 more source

Duplication cyst mimicking intestinal malrotation with volvulus: A case report

open access: yesJournal of Pediatric Surgery Case Reports, 2023
Introduction: Neonates presenting with bilious vomiting require emergent evaluation to rule out malrotation with volvulus. Enteric duplication cysts are congenital gastrointestinal lesions that can cause intestinal obstruction.
Matthew Ballweg   +3 more
doaj   +1 more source

Intestinal Malrotation Associated With Invagination of the Distal Ileum and Cancer of the Cecum: A Case Report and Literature Review

open access: yesCureus, 2021
Associated midgut malrotation and colon cancer in adult patients is extremely rare and associated with delayed diagnosis and increased morbidity. We present the case of a patient with a three-week history of weakness, diarrhea, and abdominal pain with ...
A. Taha   +4 more
semanticscholar   +1 more source

Hirschsprung disease and intestinal malrotation: A rare association with unique perioperative considerations

open access: yesJournal of Pediatric Surgery Open, 2023
Background: Multiple etiologies exist for neonatal intestinal obstruction with similar presenting symptoms. While single etiology is the most common cause, concomitant surgical diagnoses exist requiring unique peri‑operative considerations.
Dimitra M. Lotakis   +4 more
doaj   +1 more source

Intestinal Malrotation and Appendicitis in Adults [PDF]

open access: yesJurnalul de Chirurgie, 2017
Background: Intestinal malrotation is a rare condition resulting from an incomplete midgut rotation and fixation; most of the cases were diagnosed in the newborn and the presentation at adulthood is traditionally considered as rare. In the same time appendicitis is a very common surgical condition with different clinical presentations and the diagnosis
Cristina Furnica   +2 more
openaire   +1 more source

Intestinal Atresia in PPP1R12A‐Related Urogenital and Brain Malformation Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT PPP1R12A‐related urogenital and brain malformation syndrome (UBMS) is a newly described disorder characterized by congenital anomalies primarily involving the urogenital system and the brain. We describe a preterm female neonate with multiple congenital anomalies, including type IIIb jejunal atresia, incomplete intestinal rotation, imperforate
Adriana Gomes   +4 more
wiley   +1 more source

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