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警惕萎缩性胆囊——术中诊断胆囊缺如的病例报告

Beware of the shrunken gallbladder - Case report of intraoperatively diagnosed gallbladder agenesis.

作者信息

Anderson Kiyah, Roland Avery L, Miller Mark P, Foretia Denis A

机构信息

Department of Surgery, Boston Medical Center, Boston, MA, USA.

College of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Int J Surg Case Rep. 2022 Sep;98:107588. doi: 10.1016/j.ijscr.2022.107588. Epub 2022 Aug 31.

DOI:10.1016/j.ijscr.2022.107588
PMID:36058154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9482971/
Abstract

INTRODUCTION AND IMPORTANCE

Gallbladder Agenesis, the congenital absence of the gallbladder, is a very rare biliary anomaly found in 13 to 65 people per 100,000. Symptomatic patients usually present with abdominal pain, nausea, and emesis, and are often misdiagnosed with gallbladder pathologies leading to unnecessary operations.

CASE PRESENTATION

We report the case of a 63-year-old Caucasian female patient who presented with recurrent right upper quadrant pain (RUQ) and found to have a contracted gallbladder on ultrasonography (US). A hepatobiliary iminodiacetic acid (HIDA) scan was positive, and the patient was misdiagnosed with chronic cholecystitis. No gallbladder was found on laparoscopy and patient was diagnosed intraoperatively with gallbladder agenesis. Normal biliary anatomy was confirmed intraoperatively using the Firefly technique and there was no ectopic gallbladder on computed tomography (CT) scan obtained postoperatively. Patient currently doing well on conservative pain management.

CLINICAL DISCUSSION

Patients with gallbladder agenesis and normal bile ducts often have symptoms similar to that of usual gallbladder problems. Accurately diagnosing these patients preoperatively remains a challenge.

CONCLUSION

Symptomatic patients with agenesis of the gallbladder are often diagnosed intraoperatively despite major advances in diagnostic imaging techniques. In these cases, minimizing the risk of injury to the biliary tree is crucial. As our case demonstrates, it is critical for surgeons to become increasingly aware of this rare and important congenital anomaly. A very high index of suspicion is warranted in patients with a shrunken or contracted gallbladder. When in doubt, obtain cross-sectional imaging.

摘要

引言与重要性

胆囊缺如,即胆囊先天性缺失,是一种非常罕见的胆道异常,每10万人中约有13至65人发病。有症状的患者通常表现为腹痛、恶心和呕吐,常被误诊为胆囊疾病,导致不必要的手术。

病例介绍

我们报告一例63岁的白种女性患者,她反复出现右上腹疼痛(RUQ),超声检查(US)发现胆囊收缩。肝胆亚氨基二乙酸(HIDA)扫描呈阳性,患者被误诊为慢性胆囊炎。腹腔镜检查未发现胆囊,术中诊断为胆囊缺如。术中使用萤火虫技术确认胆道解剖结构正常,术后计算机断层扫描(CT)未发现异位胆囊。患者目前通过保守的疼痛管理情况良好。

临床讨论

胆囊缺如且胆管正常的患者通常有与常见胆囊问题相似的症状。术前准确诊断这些患者仍然是一个挑战。

结论

尽管诊断成像技术取得了重大进展,但有症状的胆囊缺如患者往往在术中才被诊断出来。在这些情况下,将胆管树损伤的风险降至最低至关重要。正如我们的病例所示,外科医生越来越意识到这种罕见且重要的先天性异常至关重要。对于胆囊缩小或收缩的患者,高度怀疑是必要的。如有疑问,应进行横断面成像检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/04d688e4883b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/05ea9ad394c0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/8bbe65cd0a0c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/c6766a4cd4a3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/cc7629ef2ce0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/04d688e4883b/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/05ea9ad394c0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/8bbe65cd0a0c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/c6766a4cd4a3/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/cc7629ef2ce0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a441/9482971/04d688e4883b/gr5.jpg

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