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Arrangements of Hepatobiliary Cystadenoma Complicated With Congenital Choledochal Cyst

机译:肝胆囊腺瘤并发先天性胆总管囊肿的安排

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摘要

Hepatobiliary cystadenoma complication with congenital choledochal cyst is extremely rare and has never been reported in literatures so far.The aim of the study was to investigate the disease arrangements by analyzing the case and performing a systematic review of the literature.This case report documents the details and clear patterns of the patient. A 65-year-old woman with fever (39.2°C), nausea, vomiting, and chronic hepatitis B imaging demonstrated a left hepatic multilocular cystic mass and cystic dilated common bile duct.A regular left hemihepatectomy was performed with resection of the entire tumor and choledochal cyst.The surgical margins were negative and a final diagnosis of hepatobiliary cystadenoma complicated with congenital choledochal cyst was established. The patient had an uneventful postoperative recovery and liver function returned to normal levels.Main lessons learned from this case are: the awareness should be raised about the disease to avoid misdiagnosis; preoperative ultrasonography, computed tomography, magnetic resonance imaging, and magnetic resonance cholangiopancreatography play an important role in detecting the lesion; the scope and timing of the surgery should be determined, which provide the chance of cure to complete resection of the tumor.
机译:肝胆囊腺瘤并发症并发先天性胆总管囊肿极为罕见,迄今为止尚未见文献报道。本研究的目的是通过分析病例并进行系统的文献综述来研究疾病的安排。和清楚的病人模式。一名65岁的女性,有发烧(39.2°C),恶心,呕吐和慢性乙型肝炎影像学表现,显示左肝多叶囊性肿块和胆囊扩张的胆总管,常规左半肝切除术切除了整个肿瘤手术切缘阴性,初步诊断为肝胆囊腺瘤并发先天性胆总管囊肿。患者术后恢复良好,肝功能恢复到正常水平。从该病例中学到的主要经验教训是:应提高对疾病的认识,以免引起误诊。术前超声检查,计算机断层扫描,磁共振成像和磁共振胰胆管造影在发现病变方面起着重要作用;应该确定手术的范围和时机,这为彻底切除肿瘤提供了治愈的机会。

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