Multiple Congenital Pancreatic Cysts in a Neonate

Congenital pancreatic cysts are rare in newborn babies, and this makes prenatal diagnosis difficult. Diagnosis can be delayed for a few months after birth until the infant presents with an abdominal mass, abdominal distension, or vomiting due to gastric outlet obstruction. Excision of the cyst is th...

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Bibliographic Details
Main Authors: Eun Mi Kwon (Author), Jaeho Shin (Author), Ga Won Jeon (Author)
Format: Book
Published: Korean Society of Neonatology, 2019-05-01T00:00:00Z.
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Summary:Congenital pancreatic cysts are rare in newborn babies, and this makes prenatal diagnosis difficult. Diagnosis can be delayed for a few months after birth until the infant presents with an abdominal mass, abdominal distension, or vomiting due to gastric outlet obstruction. Excision of the cyst is the treatment of choice. A congenital pancreatic cyst should be considered if the fetus has an abdominal cyst without a definite origin. A prompt diagnosis is crucial to prevent fatal complications such as cholangitis, pancreatitis, cyst rupture, and peritonitis. We report a case of neonate with multiple congenital pancreatic cysts suspected prenatally to be stomach diverticulum or duplication cysts of the intestine.
Item Description:2287-9412
2287-9803
10.5385/nm.2019.26.2.117