Lu Ying-Yi, Lai Hong-Shiee, Hsieh Wu-Shiun, Hsu Wen-Ming
Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei 100, Taiwan.
J Pediatr Surg. 2008 Jun;43(6):E31-2. doi: 10.1016/j.jpedsurg.2008.02.070.
Gallbladder perforation is an extremely rare condition in infants. We present a premature infant who had congestive heart failure and renal failure owing to complex congenital heart disease and developed gallbladder perforation at 60 days of age. The patient showed neither signs of peritonitis nor impaired liver function; however, we found bile drainage from the peritoneal dialysis tube. Emergent laparotomy revealed a 3-mm perforation with surrounding tissue necrosis over the gallbladder neck. Cholecystectomy was performed after patent common bile duct was demonstrated using intraoperative cholangiography. No stones were noted in the gallbladder. Further histologic examinations of the perforation site showed ischemic changes. There were no biliary complications after surgery. Nevertheless, the patient died of multiple organ failure at 120 days old.
胆囊穿孔在婴儿中是一种极其罕见的病症。我们报告一例早产儿,因其患有复杂先天性心脏病而出现充血性心力衰竭和肾衰竭,并在60日龄时发生了胆囊穿孔。该患者既没有腹膜炎体征,肝功能也未受损;然而,我们发现腹膜透析管有胆汁引流。急诊剖腹探查显示胆囊颈部有一个3毫米的穿孔,周围组织坏死。在术中胆管造影证实胆总管通畅后进行了胆囊切除术。胆囊内未发现结石。对穿孔部位的进一步组织学检查显示有缺血性改变。术后无胆道并发症。尽管如此,该患者在120日龄时死于多器官衰竭。