Sahu Rashmi, Quraishi Abdul Haque M, Meena Kishan Kumar, Umare Girish
General Surgery, Government Medical College & Hospital, Nagpur, IND.
Surgery, Government Medical College & Hospital, Nagpur, IND.
Cureus. 2025 May 15;17(5):e84200. doi: 10.7759/cureus.84200. eCollection 2025 May.
Agenesis of the gall bladder is extremely rare. Three types of gall bladder agenesis have been described. The asymptomatic type is diagnosed incidentally on imaging, intraoperatively, or at autopsy. Symptomatic patients present with clinical features such as biliary colic, usually in the 4th and 5th decades. The third type presents in neonatal life along with multiple fetal anomalies. We present a case of a 43-year-old male who presented to our trauma casualty with a history of multiple stab injuries to the abdomen. There was no history of previous abdominal surgery. An ultrasonography and computed tomography of the abdomen showed the absence of the gall bladder. Intraoperatively, there were multiple, through-and-through bowel perforations with no evidence of other organ injury. The gall bladder and cystic duct were absent, and the same was confirmed on a post-operative magnetic resonance cholangiopancreatography. This article emphasizes the importance of seeking and documenting incidental anatomical anomalies such as gall bladder agenesis to avoid difficulties in diagnosis if related symptoms arise in the future.
胆囊缺如极为罕见。已描述了三种类型的胆囊缺如。无症状型在影像学检查、手术中或尸检时偶然被诊断出来。有症状的患者通常在40至50岁时出现如胆绞痛等临床特征。第三种类型在新生儿期出现,并伴有多种胎儿异常。我们报告一例43岁男性患者,他因腹部多处刺伤被送至我们的创伤急诊室。既往无腹部手术史。腹部超声和计算机断层扫描显示胆囊缺如。手术中发现多处贯穿性肠穿孔,无其他器官损伤的证据。胆囊和胆囊管缺如,术后磁共振胰胆管造影也证实了这一点。本文强调了寻找并记录诸如胆囊缺如等偶然的解剖异常的重要性,以避免未来出现相关症状时诊断困难。