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胆囊缺如——腹腔镜检查中意外发现的缺失情况

Agenesis of gallbladder-an unexpected absence in laparoscopy.

作者信息

Thant Phyu C, Gupta Anurag

机构信息

Department of Surgery, Modbury Hospital, Modbury, SA, Australia.

出版信息

J Surg Case Rep. 2023 Apr 25;2023(4):rjad214. doi: 10.1093/jscr/rjad214. eCollection 2023 Apr.

DOI:10.1093/jscr/rjad214
PMID:37124577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10131097/
Abstract

Gallbladder agenesis is a very rare condition, majority of which are normally diagnosed intraoperatively because of low index of suspicion and high rate of false positive results for cholecystitis on ultrasound imaging. We present a case of a 25-year-old man who presented with a right upper quadrant pain, whose ultrasound suggests a contracted gallbladder with gallstones. He was treated as an acute on chronic cholecystitis and booked for laparoscopic cholecystectomy. Intraoperatively, there was no gallbladder to be seen and decision was made to abandon procedure and avoid further exploration. Post-operative magnetic resonance cholangiopancreatography confirmed the congenital agenesis of gallbladder. It is important to have awareness of this condition, and possible further imaging modalities should be used if the ultrasound suggests a shrunken or contracted gallbladder that is not easily visible to avoid the risk of undergoing an unwarranted surgery.

摘要

胆囊缺如是一种非常罕见的病症,由于对其怀疑指数较低且超声成像时胆囊炎的假阳性率较高,大多数病例通常在术中才得以诊断。我们报告一例25岁男性患者,其因右上腹疼痛就诊,超声检查提示胆囊萎缩并伴有胆结石。他被当作慢性胆囊炎急性发作进行治疗,并安排了腹腔镜胆囊切除术。术中未发现胆囊,于是决定放弃手术并避免进一步探查。术后磁共振胰胆管造影证实了胆囊先天性缺如。认识到这种病症很重要,如果超声提示胆囊萎缩或变小且不易看清,应考虑使用可能的进一步成像方式,以避免进行不必要手术的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/219d35a05de1/rjad214f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/af72f7be2add/rjad214f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/d78f74173d57/rjad214f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/d2f7de274269/rjad214f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/219d35a05de1/rjad214f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/af72f7be2add/rjad214f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/d78f74173d57/rjad214f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/d2f7de274269/rjad214f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fb/10131097/219d35a05de1/rjad214f4.jpg

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J Surg Case Rep. 2022 Nov 10;2022(11):rjac505. doi: 10.1093/jscr/rjac505. eCollection 2022 Nov.
2
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.
3
A Case Report on Gallbladder Agenesis: Not a Novelty but Still a Laparoscopic Surprise.
胆囊缺如病例报告:并非罕见但仍是腹腔镜手术中的意外发现
Cureus. 2021 Dec 14;13(12):e20401. doi: 10.7759/cureus.20401. eCollection 2021 Dec.
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Acute Cholecystitis-like Presentation in an Adult Patient with Gallbladder Agenesis: Case Report and Literature Review.胆囊缺如成年患者的急性胆囊炎样表现:病例报告及文献综述
Case Rep Surg. 2020 Dec 16;2020:8883239. doi: 10.1155/2020/8883239. eCollection 2020.
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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.
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Congenital agenesis of the gallbladder: a UK case report.先天性胆囊缺如:一例英国病例报告。
Oxf Med Case Reports. 2016 Aug 29;2016(8):omw040. doi: 10.1093/omcr/omw040. eCollection 2016 Aug.
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