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伴有吲哚菁绿排泄缺陷的肝细胞癌:一例报告及文献复习

Hepatocellular carcinoma with indocyanine green excretory defect: a case report and review of the literature.

作者信息

Liu Wei, Chen Li-Juan, Jiang Ying, Xu Li-Juan, Qiu Xuan

机构信息

Qingdao Haici Medical Treatment Group, Oncology Department, Qingdao, Shandong, China.

Shandong Linglong Yingcheng Hospital, Department of General Surgery, Yentai, Shandong, China.

出版信息

J Int Med Res. 2021 Apr;49(4):3000605211004025. doi: 10.1177/03000605211004025.

Abstract

Constitutional indocyanine green (ICG) excretory defect is rare. However, ICG excretory defect concomitant with hepatocellular carcinoma (HCC) is extremely rare, and only six reports of hepatectomy in patients with constitutional ICG excretory defect have been published in the English language literature through 2020. In this study, we report a case of combined HCC and ICG excretory defect and discuss its clinicopathological features and outcomes. The case featured a 68-year-old man who was admitted to the hospital with a diagnosis of resectable HCC. The preoperative ICG retention rate at 15 minutes was 82.9%. Despite this finding, the Child-Pugh assessment and hepatobiliary-specific magnetic resonance imaging (MRI) did not reveal any abnormal findings. Therefore, we diagnosed the patient with constitutional ICG excretory defect and performed partial hepatectomy. For patients requiring hepatectomy, the indications and procedure for surgery should be considered. These should be based on liver function tests such as gadolinium ethoxybenzyl diethylenetriamine pentaacetic acid-enhanced MRI.

摘要

先天性吲哚菁绿(ICG)排泄缺陷罕见。然而,ICG排泄缺陷合并肝细胞癌(HCC)极为罕见,截至2020年,英文文献中仅发表了6例关于先天性ICG排泄缺陷患者肝切除术的报告。在本研究中,我们报告1例合并HCC和ICG排泄缺陷的病例,并讨论其临床病理特征及转归。该病例为一名68岁男性,因诊断为可切除HCC入院。术前15分钟ICG潴留率为82.9%。尽管有此发现,但Child-Pugh评估及肝胆特异性磁共振成像(MRI)未显示任何异常发现。因此,我们诊断该患者为先天性ICG排泄缺陷,并实施了部分肝切除术。对于需要肝切除术的患者,应考虑手术指征及手术方式。这些应基于诸如钆塞酸二钠增强MRI等肝功能检查结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e619/8047085/9cd5afc7fe56/10.1177_03000605211004025-fig1.jpg

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