Cavazos-García Ricardo, Díaz-Elizondo José Antonio, Flores-Villalba Eduardo, Rodríguez-García Héctor Alejandro
Cirugía General, Programa Multicéntrico de Residencias Médicas, Escuela de Medicina y Ciencias de la Salud del Tecnológico de Monterrey, Monterrey, Nuevo León, México.
Cirugía General, Programa Multicéntrico de Residencias Médicas, Escuela de Medicina y Ciencias de la Salud del Tecnológico de Monterrey, Monterrey, Nuevo León, México.
Cir Cir. 2015 Sep-Oct;83(5):424-8. doi: 10.1016/j.circir.2015.05.043. Epub 2015 Jul 7.
Gallbladder agenesis is a very rare congenital abnormality of the biliary tract. The diagnosis is made during surgery, because all preoperative studies have failed to identify this malformation. The purpose of this article is to present a case of gallbladder agenesis diagnosed during surgery, its management, and a review of the literature.
The case involves a sixty-two year- old female, referring to repeated biliary colic symptoms. The abdominal ultrasound diagnosed cholelithiasis. It was impossible to identify the gallbladder during surgery. Diagnosis was confirmed by intra-operative cholangiography.
Preoperative diagnostic workup has failed to recognise patients with gallbladder agenesis. It is currently recommended to abandon the surgery once this diagnosis is suspected and confirm it by a cholangio-magnetic resonance scan in order to avoid a bile duct injury.
Agenesis of the gallbladder is a rare congenital abnormality of the biliary tree. Every surgeon must keep this rare entity in mind when a "difficult dissection" or an anatomic variant is identified during surgery, and make use of an intra-operative cholangiography, mainly to prevent a bile duct injury.
胆囊缺如是一种非常罕见的先天性胆道异常。诊断通常在手术过程中做出,因为所有术前检查都未能识别出这种畸形。本文旨在介绍一例在手术中诊断出的胆囊缺如病例、其处理方法以及文献综述。
该病例为一名62岁女性,反复出现胆绞痛症状。腹部超声诊断为胆结石。手术中无法识别胆囊。术中胆管造影证实了诊断。
术前诊断检查未能识别出胆囊缺如的患者。目前建议一旦怀疑该诊断,应放弃手术,并通过胆管磁共振扫描加以确认,以避免胆管损伤。
胆囊缺如是一种罕见的先天性胆管树异常。每位外科医生在手术中遇到“困难解剖”或解剖变异时,都必须牢记这种罕见情况,并利用术中胆管造影,主要是为了防止胆管损伤。