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Multiple Congenital Pancreatic Cysts in a Neonate

  • Kwon, Eun Mi (Department of Pediatrics, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Shin, Jaeho (Division of Pediatric Surgery, Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine) ;
  • Jeon, Ga Won (Department of Pediatrics, Inje University Busan Paik Hospital, Inje University College of Medicine)
  • Received : 2018.08.30
  • Accepted : 2019.01.29
  • Published : 2019.05.28

Abstract

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.

Keywords

References

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