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腹腔镜诊断的胆囊和胆囊管先天性畸形:手术风险高。

Congenital malformations of the gallbladder and cystic duct diagnosed by laparoscopy: high surgical risk.

作者信息

Carbajo M A, Martín del Omo J C, Blanco J I, Cuesta C, Martín F, Toledano M, Atienza R, Vaquero C

机构信息

Department of General and Digestive Surgery Medina del Campo Hospital, Valladolid, Spain.

出版信息

JSLS. 1999 Oct-Dec;3(4):319-21.

Abstract

Congenital anomalies of the gallbladder are rare and can be accompanied by other malformations of the biliary or vascular tree. Being difficult to diagnose during routine preoperative studies, these anomalies can provide surgeons with an unusual surprise during laparoscopic surgery. The presence of any congenital anomaly or the mere suspicion of its existence demands that we exercise surgical prudence, limit the use of electrocoagulation, and ensure that no structure be divided until a clear picture of the bile ducts and blood vessels is obtained. If necessary, perform intraoperative cholangiography to further define the biliary system. However, if the case remains unclear, or if laparoscopy does not provide enough information, open surgery should be considered before undesirable complications occur.

摘要

胆囊先天性异常较为罕见,可伴有胆道或血管系统的其他畸形。由于这些异常在常规术前检查中难以诊断,在腹腔镜手术过程中可能会给外科医生带来意外。任何先天性异常的存在或仅仅是怀疑其存在,都要求我们在手术中保持谨慎,限制电凝的使用,并确保在清晰了解胆管和血管结构之前不切断任何结构。如有必要,进行术中胆管造影以进一步明确胆道系统。然而,如果情况仍不明确,或者腹腔镜检查未能提供足够信息,应在出现不良并发症之前考虑开放手术。

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