Hyperamylasemia, duodenal duplication, and pleural effusions in hereditary spherocytosis

Digestive Diseases and Sciences
P E HymanD M McCarthy

Abstract

A 15-year-old girl with hereditary spherocytosis was admitted for evaluation of recurrent pleural effusions containing amylase in high concentration and was found to have biliary obstruction, pancreatitis, and a congenital duplication of the duodenum attached to an accessory lobe of the pancreas via the duct of Santorini, a unique entity. Successful surgical management of these disorders included common duct clearance and anastomosis of the duplication to the adjacent duodenum.

References

Aug 1, 1977·The Journal of Pediatrics·S C Jordan, M E Ament
Mar 1, 1960·The British Journal of Surgery·R BASUP P RICKHAM
Apr 1, 1965·Archives of Disease in Childhood·W H HENDRENA S PATTON
Dec 28, 2005·The American Journal of Medicine·Matthew E FalagasPetros Kopterides

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Citations

Jul 1, 1984·The Japanese Journal of Surgery·H ShimadaS Morita
Sep 28, 2002·Journal of Pediatric Gastroenterology and Nutrition·Hisayoshi KawaharaAkira Okada
Mar 1, 1993·The Australian and New Zealand Journal of Surgery·K Y NgN Collier

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