Ji Guwei, Zhu Feipeng, Wang Ke, Jiao Chenyu, Shao Zicheng, Li Xiangcheng
Liver Transplantation Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, P.R. China.
Department of Radiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, P.R. China.
Mol Clin Oncol. 2017 Jan;6(1):71-74. doi: 10.3892/mco.2016.1075. Epub 2016 Nov 8.
Gallbladder perforation (GBP) represents a rare, but potentially life-threatening, complication of acute cholecystitis. GBP is subdivided into three categories whereas the development of biloma is extremely rare. The present case study reports on a 40-year-old man with a 10-year history of calculus cholecystitis, who was referred to The First Affiliated Hospital of Nanjing Medical University (Nanjing, China) for the surgical treatment of an emerging massive hepatic entity with insidious symptoms and normal laboratory tests. A preoperative imaging study demonstrated the collection with internal septations and mural nodules, but no visible communication with the biliary system. Given the suspected biliary cystic tumor, a laparotomy was performed and the lumen was scattered with papillae. An intraoperative frozen section examination illustrated a simple hepatic cyst. Biochemical analysis of the collection and histopathology of the gallbladder and capsule substantiated the diagnosis of biloma formation due to GBP. The purpose of the present case report was to demonstrate how a pinhole-sized perforation with extravasation of unconcentrated bile from the gallbladder may result in insidious clinical presentation and an undetected leak site. According to the clinicopathological characteristics and composition, formation of biloma should be classified as type IV GBP. To differentiate bilomas with intracystic septations and mural nodules from BCTs is difficult via a preoperative examination, and the definitive diagnosis should be based on a histological examination. Laparotomy with frozen section examination may be the optimal approach in such a case.
胆囊穿孔(GBP)是急性胆囊炎一种罕见但可能危及生命的并发症。GBP可分为三类,而胆汁瘤的形成极为罕见。本病例研究报告了一名40岁男性,有10年结石性胆囊炎病史,因出现症状隐匿且实验室检查正常的巨大肝脏肿物而被转诊至南京医科大学第一附属医院(中国南京)接受手术治疗。术前影像学检查显示肿物内有分隔及壁结节,但与胆道系统无明显相通。鉴于怀疑为胆管囊性肿瘤,遂行剖腹手术,发现腔内布满乳头状物。术中冰冻切片检查显示为单纯性肝囊肿。对肿物进行生化分析以及对胆囊和包膜进行组织病理学检查,证实诊断为GBP导致的胆汁瘤形成。本病例报告的目的是展示胆囊一个针孔大小的穿孔伴未浓缩胆汁外渗如何导致隐匿的临床表现及未被发现的渗漏部位。根据临床病理特征和成分,胆汁瘤的形成应归类为IV型GBP。术前检查很难将有囊内分隔和壁结节的胆汁瘤与胆管囊性肿瘤区分开来,明确诊断应基于组织学检查。在这种情况下,剖腹手术加冰冻切片检查可能是最佳方法。