Balzan Silvio, Kianmanesh Reza, Farges Olivier, Sauvanet Alain, O'toole Dermot, Levy Philippe, Ruszniewski Philippe, Ogata Satoshi, Belghiti Jacques
Department of Hepato-Pancreatico-Biliary Surgery, Hospital Beaujon, 92110, Clichy, France.
J Hepatobiliary Pancreat Surg. 2005;12(2):135-7. doi: 10.1007/s00534-004-0929-0.
The location of a pseudocyst (PC) in the liver is an exceptional event, and intrahepatic PCs are mainly located in the left lobe. We report here a case of right intrahepatic PC following acute pancreatitis associated with cystic (aberrant pancreatic) dystrophy of the duodenal wall (CDDW) and chronic pancreatitis. Morphological assessment (ultrasound, computed tomography [CT] scan, and cholangio-magnetic resonance imaging [MRI]) revealed a 10-cm right intrahepatic collection and rupture of the main pancreatic duct. Percutaneous puncture permitted us to detect a high level of amylase in the collection, confirming the diagnosis of intrahepatic PC. Surgical drainage concomitant with pancreatico-duodenectomy for the treatment of CDDW resulted in disappearance of the collection. The mechanism involved in this patient was rupture of the pancreatic duct in the retroperitoneal cavity and erosion reaching the right hepatic parenchyma. Although intrahepatic PCs are rare, the diagnosis of intrahepatic PC complicating acute pancreatitis can be confirmed by a high level of amylase in the collection. Asymptomatic intrahepatic PCs can be treated conservatively, and symptomatic intrahepatic PCs can be managed either transcutaneously or surgically.
肝内假性囊肿(PC)的位置较为罕见,肝内PC主要位于左叶。我们在此报告一例急性胰腺炎后并发十二指肠壁囊性(异位胰腺)营养不良(CDDW)和慢性胰腺炎的右肝内PC病例。形态学评估(超声、计算机断层扫描[CT]和胆管磁共振成像[MRI])显示右肝内有一个10厘米的积液区以及主胰管破裂。经皮穿刺使我们在积液中检测到高水平的淀粉酶,从而确诊为肝内PC。针对CDDW进行胰十二指肠切除术并同时进行手术引流后,积液消失。该患者的发病机制为胰管在腹膜后腔破裂并侵蚀至右肝实质。尽管肝内PC罕见,但通过积液中高水平的淀粉酶可确诊急性胰腺炎并发肝内PC。无症状的肝内PC可保守治疗,有症状的肝内PC可通过经皮或手术方式处理。