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肝内 VII 型胆总管囊肿:放射学见解与手术入路。

Intrahepatic Class VII Choledochal Cyst: Radiological Insights and Surgical Approach.

机构信息

Department of Surgery, Faculty of Medicine, Al-Baha University, Al-Baha, Saudi Arabia.

出版信息

Am J Case Rep. 2024 Dec 1;25:e945049. doi: 10.12659/AJCR.945049.

Abstract

BACKGROUND Choledochal cysts are congenital cystic dilatation of any section of the bile ducts. They have been divided into 5 primary categories. This is the case of an intrahepatic variant of bile duct cysts originating from the main lobar bile ducts at the confluence, initially radiologically identified as biliary cystadenoma in segments 4b and 5. CASE REPORT A 35-year-old woman presented with right upper quadrant pain and palpable mass during examination. History and laboratory results were normal. Magnetic resonance cholangiopancreatography revealed a complicated cystic lesion compressing right and left proximal hepatic ducts, diagnosed radiologically as biliary cyst adenoma in segments 4b and 5. Intraoperatively, large cyst found in liver segment 4b and 5, extending infra-hepatic, included the confluence of the common hepatic duct and extended to the gallbladder. It was easily separable from the gallbladder, and total cholecystectomy was done; however, the cyst was inseparable from the confluence of common hepatic duct. The peritoneum over the cyst, containing the right and left hepatic duct and in the area of confluence, was dissected and pushed down to avoid injury; enucleation of the lower border was successfully done. Upper border was transected through liver parenchyma; many small ductules connected with the cyst were ligated. Resection should be done to decrease possibility of malignant transformation and prevent recurrent cholangitis. CONCLUSIONS Class VII choledochal cyst is rare, and surgery is the preferred choice, after proper evaluation of the cyst and surrounding structure. Magnetic resonance cholangiopancreatography still has a high overall accuracy for choledochal cyst diagnosis and classification.

摘要

背景

胆总管囊肿是胆管的任何节段先天性囊状扩张。它们已分为 5 个主要类别。这是一个源于汇合处主要叶状胆管的肝内胆管囊肿的变异病例,最初在影像学上被确定为 4b 和 5 段的胆管囊腺瘤。

病例报告

一名 35 岁女性因右上腹疼痛和体检时可触及肿块就诊。病史和实验室结果正常。磁共振胰胆管成像显示一个复杂的囊性病变压迫右和左近端肝管,影像学诊断为 4b 和 5 段的胆管囊腺瘤。术中发现肝段 4b 和 5 内有一个大囊肿,向下延伸至肝外,包括肝总管汇合处并延伸至胆囊。它很容易与胆囊分离,因此进行了胆囊全切除术;然而,囊肿与肝总管汇合处无法分离。沿囊肿表面的腹膜,包含右和左肝管并在汇合处区域,被分离并向下推以避免损伤;成功地进行了下边界的剜除。上边界通过肝实质横断;与囊肿相连的许多小胆管被结扎。为了降低恶性转化的可能性并预防复发性胆管炎,应进行切除。

结论

VII 型胆总管囊肿罕见,在对囊肿和周围结构进行适当评估后,手术是首选。磁共振胰胆管成像对胆总管囊肿的诊断和分类仍具有较高的总体准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd03/11622327/c0d19d4bf13a/amjcaserep-25-e945049-g001.jpg

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