Results 11 to 20 of about 2,702 (168)
Patent Omphalomesenteric Duct [PDF]
A full-term newborn male, a product of elective cesarean section, presented with drainage of meconium from the umbilical stump within the first few minutes of life (Panel A).
Zuhair Easa, Rana Shitran
doaj +1 more source
This is the first study assessing the cytoarchitecture of the vitellarium of members of the freshwater, teleost-infecting lineage of blood-flukes (Aporocotylidae).
Poddubnaya Larisa G. +2 more
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Intestinal prolape of an omphalo-mesenteric fistula
Intestinal prolapse through a persistence of the omphalo-mesenteric duct or vitelline duct is a very rare clinical entity. It is a complication of the omphalo-mesenteric fistula which requires emergency surgery.
Bénié Adoubs Célestin +6 more
doaj +1 more source
The persistent vitellointestinal duct (PVID) is the rarest of all the vitelline duct anomalies. The enteric end of the vitelline duct mostly connects to the terminal ileum.
Rajendra Kumar Ghritlaharey
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Duplication of the portal vein is a rare variation, and reports of this condition are quite limited. The present report describes a woman of advanced age who was incidentally diagnosed with duplicated portal veins.
Toshihide Yamaoka, MD, PhD
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The persistent vitellointestinal duct is the rarest of all vitelline duct anomalies. This systematic literature review was undertaken to investigate and review the demographics, clinical presentation, surgical procedure performed, and outcome of infants ...
Rajendra K. Ghritlaharey
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Omphalomesenteric duct & Urachal remnant presentation in a newborn
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, C. Mizzi, N. Gatt, J. Galea
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Spontaneous Rupture of Adenocarcinoma of Meckel’s Diverticulum- A Rare Entity [PDF]
Meckel’s diverticulum is a true diverticulum from remnant of vitelline duct. It is most common congenital anomaly of intestine. It is associated with intestinal atresia and anorectal anomalies. It contains heterotrophic epithelium.
Jayabal Pandiaraja
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A rare combination of congenital anomalies following in utero methimazole exposure
The use of methimazole for the treatment of hyperthyroidism in the first trimester of pregnancy has been linked to several congenital malformations. Most commonly reported is choanal atresia; however, other anomalies have been described including aplasia
Taylor Shaw +4 more
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Omphalomesenteric Fistula Presenting with Meconium Discharge from the Umbilicus
The omphalomesenteric duct is an embryologic connection between the midgut and yolk sac, which typically disappears at 5th to 7th week of gestation. Failure of the obliteration process can lead to omphalomesenteric duct remnants.
Yun-Hee Lee +3 more
doaj +1 more source

