Gross E-type congenital esophageal atresia associated with congenital esophageal stenosis is extremely rare. In a male infant born at 36 weeks of gestation, bubbly vomiting was noted after birth. X-ray films of the ch...Gross E-type congenital esophageal atresia associated with congenital esophageal stenosis is extremely rare. In a male infant born at 36 weeks of gestation, bubbly vomiting was noted after birth. X-ray films of the chest and abdomen showed coil-up sign of the nasogastric tube and gas in the stomach and small intestines were recognized, so gross C-type esophageal atresia was suspected and surgery was performed on the first day of life. Surgery revealed the presence of a tracheoesophageal fistula in the upper esophagus and membranous stenosis on the distal side.展开更多
Traumatic rupture of choledochal cyst is an extremely rare disorder.The current patient is a 4-year-old boy who fell in a bathroom and suffered a blow to the abdomen.Percutaneous transhepatic cholangiography revealed ...Traumatic rupture of choledochal cyst is an extremely rare disorder.The current patient is a 4-year-old boy who fell in a bathroom and suffered a blow to the abdomen.Percutaneous transhepatic cholangiography revealed pancreaticobiliary maljunction.Inflammation of the peritoneal cavity was moderate.At first look, the choledochal cyst was excised and hepaticojejunostomy was performed.At this time, a rupture approximately 2 mm in diameter was recognized at the rear surface of the inferior part of the common bile duct.展开更多
文摘Gross E-type congenital esophageal atresia associated with congenital esophageal stenosis is extremely rare. In a male infant born at 36 weeks of gestation, bubbly vomiting was noted after birth. X-ray films of the chest and abdomen showed coil-up sign of the nasogastric tube and gas in the stomach and small intestines were recognized, so gross C-type esophageal atresia was suspected and surgery was performed on the first day of life. Surgery revealed the presence of a tracheoesophageal fistula in the upper esophagus and membranous stenosis on the distal side.
文摘Traumatic rupture of choledochal cyst is an extremely rare disorder.The current patient is a 4-year-old boy who fell in a bathroom and suffered a blow to the abdomen.Percutaneous transhepatic cholangiography revealed pancreaticobiliary maljunction.Inflammation of the peritoneal cavity was moderate.At first look, the choledochal cyst was excised and hepaticojejunostomy was performed.At this time, a rupture approximately 2 mm in diameter was recognized at the rear surface of the inferior part of the common bile duct.
