Annular pancreas in identical twin newborns

Annular pancreas is a rare congenital anomaly occurring in 1 of every 12,000 to 15,000 live births [Nerwich N, Shi E. Neonatal duodenal obstruction: a review of 30 consecutive cases. Pediatr Surg Int 1994;9:47-50]. It may remain asymptomatic throughout life, present in adulthood, or present in infan...

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Veröffentlicht in:Journal of pediatric surgery 2006-08, Vol.41 (8), p.e19-e21
Hauptverfasser: Hulvat, Melissa C., Kumar, Rajiv B., Newman, Barry M., Muraskas, Jonathan K.
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Sprache:eng
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Zusammenfassung:Annular pancreas is a rare congenital anomaly occurring in 1 of every 12,000 to 15,000 live births [Nerwich N, Shi E. Neonatal duodenal obstruction: a review of 30 consecutive cases. Pediatr Surg Int 1994;9:47-50]. It may remain asymptomatic throughout life, present in adulthood, or present in infancy as a high intestinal obstruction. Review of the literature demonstrates only 8 cases of familial annular pancreas and no case of twins exhibiting the disease. We will describe a case of identical (monochorionic diamniotic) female twins with neonatal presentation of duodenal obstruction and annular pancreas, and discuss data supportive of a genetic etiology.
ISSN:0022-3468
1531-5037
DOI:10.1016/j.jpedsurg.2006.04.028