Duplicated gallbladder: an incidental anatomical variation in a patient with symptomatic cholelithiasis

Q4 Dentistry
Ludmila Baltaga, Dimosthenis Chrysikos, Spiros Delis, Charina Triantopoulou, Dimitrios Filippou, Vasileios Protogerou, Theodore Troupis
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引用次数: 0

Abstract

Congenital malformations of the biliary tract represent a relatively rare entity with which surgeons, radiologists and clinicians are not adequately familiarized. We present a rare case of gallbladder duplication in a 40-year-old female, with the accessory cystic duct entering the left hepatic duct, which depicts the fifth reported case in the international bibliography. Our case illustrates the importance of detailed knowledge of anatomical malformations of the biliary tree, serving the purpose of a preoperative diagnosis of symptomatic cholelithiasis. It is also of paramount importance to take under consideration biliary tract malformations to avoid inadvertent complications such as biliary duct injuries in case of laparoscopic cholecystectomy.
胆囊重复:有症状的胆石症患者的偶然解剖变异
胆道先天性畸形是一种相对罕见的疾病,外科医生、放射科医生和临床医生对其都不太熟悉。我们提出一个罕见的病例胆囊重复,在一个40岁的女性,副胆囊管进入左肝管,这是在国际文献中报道的第五例病例。我们的病例说明了详细了解胆道树解剖畸形的重要性,有助于症状性胆石症的术前诊断。在腹腔镜胆囊切除术中,考虑到胆道的畸形,以避免胆道损伤等意外并发症也是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Folia medica
Folia medica Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
121
审稿时长
5 weeks
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