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重复胆囊的磁共振胰胆管造影成像:一例病例报告及文献复习

MRCP imaging of duplicate gallbladder: a case report and review of the literature.

作者信息

Botsford Alex, McKay Kathy, Hartery Angus, Hapgood Connie

机构信息

Discipline of Radiology, Faculty of Medicine, Janeway Child Health Centre, Memorial University of Newfoundland, St. John's, NL, A1B 3V6, Canada,

出版信息

Surg Radiol Anat. 2015 Jul;37(5):425-9. doi: 10.1007/s00276-015-1456-1. Epub 2015 Mar 11.

Abstract

PURPOSE

Duplicate gallbladder is a rare congenital abnormality of the hepatobiliary system that has an incidence of roughly 1 in 4000. Many surgical studies have demonstrated that congenital anomalies of the gallbladder and anatomical variations of its position are associated with an increased risk of complications after laparoscopic cholecystectomy.

METHODS

Using ultrasound, MRCP and 3D reconstructions, we report a case of a 29-year-old female who was incidentally revealed to have a duplicated gallbladder. A review of the literature surrounding this variant, its anatomical classifications and relevance to surgical practice is included.

CONCLUSION

The double gallbladder is a rare congenital condition that is often not considered in the differential diagnosis for a patient with gallbladder disease or intraoperatively. At present, it is only detected via pre-operative imaging in 50% of cases, but an understanding of the limitations of ultrasound combined with more frequent and thorough use of MRCP before surgical intervention could prevent serious complications of laparoscopy in these patients.

摘要

目的

重复胆囊是一种罕见的肝胆系统先天性异常,发病率约为四千分之一。许多外科研究表明,胆囊先天性异常及其位置的解剖变异与腹腔镜胆囊切除术后并发症风险增加有关。

方法

我们通过超声、磁共振胰胆管造影(MRCP)和三维重建技术,报告了一例29岁女性偶然发现重复胆囊的病例。文中还回顾了关于该变异、其解剖学分类以及与外科手术相关性的文献。

结论

双胆囊是一种罕见的先天性疾病,在胆囊疾病患者的鉴别诊断中或术中通常未被考虑。目前,仅50%的病例通过术前影像学检查发现,但在手术干预前了解超声的局限性并更频繁、全面地使用MRCP,可预防这些患者腹腔镜手术的严重并发症。

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