Diaconu Georgian, Martiniuc Alexandru, Lupescu Ioana, Ceauşu Mihai, Dumitraşcu Traian
Chirurgia (Bucur). 2019 Jan-Feb;114(1):121-125. doi: 10.21614/chirurgia.114.1.121.
Agenesis of the right liver is a rare congenital anomaly which can be associated with an ectopic gallbladder. Hereby, it is presented the case of a 39-year-old man investigated for right upper quadrant abdominal pain and diagnosed at computed tomography with a cystic liver mass initially considered as hydatid cyst. At laparotomy, it was discovered agenesis of the right liver and the presumed hydatid cyst was a retrohepatic gallbladder with lithiasis. Cholecystectomy was performed with an uneventful outcome. Reassessment of the computed tomography images by an experienced radiologist confirmed the intraoperative diagnosis. Although agenesis of the right liver with retrohepatic gallbladder is an exceptional appearance, surgeons should be aware of this anomaly because it can raise challenging issues of diagnosis and surgical planning during cholecystectomy.
右肝缺如是一种罕见的先天性异常,可伴有异位胆囊。在此,报告一例39岁男性,因右上腹疼痛接受检查,计算机断层扫描诊断为肝脏囊性肿块,最初被认为是包虫囊肿。剖腹手术时,发现右肝缺如,推测的包虫囊肿是一个伴有结石的肝后胆囊。行胆囊切除术,术后恢复顺利。一位经验丰富的放射科医生对计算机断层扫描图像进行重新评估,证实了术中诊断。虽然右肝缺如伴肝后胆囊是一种罕见的表现,但外科医生应意识到这种异常,因为在胆囊切除术中它可能会引发诊断和手术规划方面的挑战性问题。