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胆囊缺如:一例刺伤病例术中偶然发现

Gall Bladder Agenesis: An Incidental Intraoperative Finding in a Case of Stab Injury.

作者信息

Sahu Rashmi, Quraishi Abdul Haque M, Meena Kishan Kumar, Umare Girish

机构信息

General Surgery, Government Medical College & Hospital, Nagpur, IND.

Surgery, Government Medical College & Hospital, Nagpur, IND.

出版信息

Cureus. 2025 May 15;17(5):e84200. doi: 10.7759/cureus.84200. eCollection 2025 May.

DOI:10.7759/cureus.84200
PMID:40524997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12168724/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/ba621b44de22/cureus-0017-00000084200-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/f39a107c06d0/cureus-0017-00000084200-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/64b4ff546b97/cureus-0017-00000084200-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/414926022a49/cureus-0017-00000084200-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/ba621b44de22/cureus-0017-00000084200-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/f39a107c06d0/cureus-0017-00000084200-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/64b4ff546b97/cureus-0017-00000084200-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/414926022a49/cureus-0017-00000084200-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1378/12168724/ba621b44de22/cureus-0017-00000084200-i04.jpg

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本文引用的文献

1
Duplicated gallbladder with acute cholecystitis: a case of unusual presentation and diagnostic challenges.重复胆囊伴急性胆囊炎:一例不寻常表现及诊断挑战的病例
World J Emerg Med. 2024;15(2):156-158. doi: 10.5847/wjem.j.1920-8642.2024.021.
2
Agenesis of gallbladder-an unexpected absence in laparoscopy.胆囊缺如——腹腔镜检查中意外发现的缺失情况
J Surg Case Rep. 2023 Apr 25;2023(4):rjad214. doi: 10.1093/jscr/rjad214. eCollection 2023 Apr.
3
Gallbladder agenesis a rare and underdiagnosed congenital anomaly: a case report and literature review.
胆囊缺如:一种罕见且诊断不足的先天性异常——病例报告及文献综述
J Surg Case Rep. 2022 Nov 10;2022(11):rjac505. doi: 10.1093/jscr/rjac505. eCollection 2022 Nov.
4
Beware of the shrunken gallbladder - Case report of intraoperatively diagnosed gallbladder agenesis.警惕萎缩性胆囊——术中诊断胆囊缺如的病例报告
Int J Surg Case Rep. 2022 Sep;98:107588. doi: 10.1016/j.ijscr.2022.107588. Epub 2022 Aug 31.
5
Case report of a gallbladder agenesis, a diagnostic challenge.胆囊缺如病例报告:一项诊断挑战
Int J Surg Case Rep. 2022 May;94:107026. doi: 10.1016/j.ijscr.2022.107026. Epub 2022 Apr 4.
6
Gallbladder Agenesis Mimicking Chronic Cholecystitis in a Young Woman.一名年轻女性中酷似慢性胆囊炎的胆囊缺如
Cureus. 2021 Sep 23;13(9):e18222. doi: 10.7759/cureus.18222. eCollection 2021 Sep.
7
Gallbladder agenesis: A case report and review of the literature.胆囊发育不全:一例病例报告及文献综述
Int J Surg Case Rep. 2018;53:235-237. doi: 10.1016/j.ijscr.2018.10.061. Epub 2018 Nov 1.
8
Gallbladder Agenesis: A Case Report.胆囊缺如:一例报告
Yale J Biol Med. 2018 Sep 21;91(3):237-241. eCollection 2018 Sep.
9
Gall Bladder Agenesis: A Rare Embryonic Cause of Recurrent Biliary Colic.胆囊缺如:复发性胆绞痛的一种罕见胚胎学病因。
Am J Case Rep. 2017 Apr 2;18:334-338. doi: 10.12659/ajcr.903176.
10
The diagnosis of gallbladder agenesis: two cases report.胆囊缺如的诊断:两例报告
Int J Clin Exp Med. 2015 Feb 15;8(2):3010-6. eCollection 2015.