Yener Oktay, Buldanlı Mehmet Zeki, Eksioglu Hayati, Leblebici Metin, Alimoglu Orhan
Faculty of Medicine, Istanbul Medeniyet University, Göztepe Training and Research Hospital, Istanbul, Turkey.
Prague Med Rep. 2015;116(1):52-6. doi: 10.14712/23362936.2015.46.
Gallbladder agenesis (GA) is a rare congenital anomaly of the biliary system often associated with other congenital abnormalities. Patients become symptomatic in 23% of cases (Richards et al., 1993). GA is often misinterpreted as other diseases, therefore, leading to unnecessary surgery. Many of these patients develop a typical symptomatology of cholelithiasis that leads them to operating theatre. If an operative procedure is done, it is better to remain at the level of laparoscopy because further surgical investigation may lead to detrimental biliary tract injuries (Waisberg et al., 2002). We present a case of GA, diagnosed by magnetic resonance with cholangiopancreatography.
胆囊缺如(GA)是一种罕见的胆道系统先天性异常,常与其他先天性畸形相关。23%的病例中患者会出现症状(理查兹等人,1993年)。GA常被误诊为其他疾病,因此导致不必要的手术。许多这类患者会出现典型的胆石症症状,从而导致他们进入手术室。如果进行手术操作,最好停留在腹腔镜检查层面,因为进一步的手术探查可能导致有害的胆道损伤(魏斯伯格等人,2002年)。我们报告一例通过磁共振胰胆管造影诊断的GA病例。