choledochal cyst/asthenia

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Spontaneous perforation of choledochal cyst: a study of 13 cases.

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Of the 187 cases of infantile choledochal cyst treated at our hospitals, we encountered 13 with spontaneous perforation. All cases were under 4 years old. Eight cases were found to have biliary peritonitis and 5 had a sealed perforation. The shape of the extrahepatic bile duct was cystic in 8 and

Spontaneous rupture of extrahepatic choledochal cyst: two pediatric cases and literature review.

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Spontaneous rupture of extrahepatic choledochal cysts is very rare. Neonatal cases generally present with biliary ascites, and older children with acute abdomen. Although the cause is unclear, accumulation of protein plugs in an anomalous pancreaticobiliary junction, irritation of the cyst wall due

Lessons and tips from the experience of pediatric robotic choledochal cyst resection.

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OBJECTIVE The laparoscopic surgery for a choledochal cyst in children is technically challenging because of its high degree of complexity despite its possibility. In an attempt to overcome this laparoscopic weakness and to facilitate the difficult steps in the minimally invasive surgery for

A clinicopathologic study of choledochal cyst.

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Choledochal cyst is quite common in Japan. The etiology of this lesion is not clear, and there remain problems in its treatment as well. Radiologic investigation of the distal common bile and pancreatic ducts was performed by operative cholangiography and endoscopic retrograde

[Dynamics of individual cardiovascular reactions in rabbits during acute experimental emotional stress].

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Recently the so-called anomalous arrangement of the pancreatico-biliary duct has often been found in congenital choledochal cyst. This anomaly was also observed in all of our 11 cases in which cholangiograms demonstrated the lower portion of the common bile duct. Therefore, this anomaly has been

[Etiopathogenic study of spontaneous perforation of the biliary tract].

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Spontaneous perforation of extrahepatic bile duct is a rare entity, but is the second cause of surgical jaundice in the newborn period after biliary atresia. We review the etiological theories and three patients with this anomaly. Centrolobulillar cholestasis was present in all cases. Parietal

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