Balakrishnan Santosh, Singhal Tarun, Grandy-Smith Starlene, El-Hasani Shamsi
Department of Surgery, The Princess Royal University Hospital, Bromley Hospitals, Orpington, Kent, United Kingdom.
JSLS. 2006 Oct-Dec;10(4):517-9.
Congenital absence of the gallbladder is a rare, usually asymptomatic, anatomical variation. Some affected individuals may present with a clinical picture suggestive of gallbladder disease. This presentation, coupled with the inability of standard abdominal ultrasonography to convincingly diagnose agenesis of the gallbladder, can put the surgeon in a diagnostic and intraoperative dilemma.
A 30-year-old lady presenting with clinical features of cholecystitis and diagnosed with shrunken gallbladder on ultrasonography was scheduled for laparoscopic cholecystectomy. Intraoperatively, the gallbladder could not be seen even after thorough dissection in the region of the porta hepatis. The procedure was terminated at this stage, and further imaging of the extrahepatic biliary system by magnetic resonance cholangiopancreatography and endoscopic ultrasound confirmed the diagnosis of congenital absence of the gallbladder.
Nonvisualization of the gallbladder at laparoscopy, in the absence of any other diagnosed biliary disorder, need not prompt conversion to open exploration of the extrahepatic biliary system. Newer imaging modalities are relatively noninvasive and can provide good delineation of biliary anatomy. This allows wellplanned treatment and at the same time prevents the added morbidity of a diagnostic laparotomy performed solely to confirm the absence of the gallbladder.
先天性胆囊缺如是一种罕见的、通常无症状的解剖变异。一些受影响的个体可能表现出提示胆囊疾病的临床症状。这种表现,再加上标准腹部超声无法令人信服地诊断胆囊缺如,可能会使外科医生陷入诊断和术中的两难境地。
一名30岁女性,表现出胆囊炎的临床特征,超声检查诊断为胆囊萎缩,计划行腹腔镜胆囊切除术。术中,即使在肝门区域进行了彻底解剖,仍未发现胆囊。此时手术终止,通过磁共振胰胆管造影和内镜超声对肝外胆管系统进行进一步成像,证实了先天性胆囊缺如的诊断。
在腹腔镜检查时未发现胆囊,且无其他已诊断的胆道疾病,不必立即转为对肝外胆管系统进行开放探查。更新的成像方式相对无创,能够很好地显示胆道解剖结构。这有助于进行精心规划的治疗,同时避免了仅为确认胆囊缺如而进行诊断性剖腹手术所增加的发病率。