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9例吲哚菁绿试验明显潴留且磺溴酞钠试验正常,肝脏组织学无异常:体质性吲哚菁绿排泄缺陷。

Nine cases with marked retention of indocyanine green test and normal sulfobromophthalein test without abnormal liver histology: constitutional indocyanine green excretory defect.

作者信息

Namihisa T, Nambu M, Kobayashi N, Kuroda H

出版信息

Hepatogastroenterology. 1981 Feb;28(1):6-12.

PMID:7216141
Abstract

Nine patients revealed marked retention in the indocyanine green (ICG) test and the normal sulfobromophthalein (BSP) test. The results of liver function tests in these cases were within normal limits with the exception of the ICG test. The ICG plasma disappearance rate ranged from 0.017 to 0.025, whereas that of BSP ranged from 0.058 to 0.126. The transfer rate of ICG from plasma to liver markedly decreased on two-compartmental analysis of the ICG decay curve. A transient delay of the ICG plasma disappearance (step formation) on the decay curve was observed over 20 to 25 minutes after an injection in all cases after repeated observation. Binding of ICG to plasma proteins in these cases failed to demonstrate a significant difference from normal subjects. The fasting serum bile acid levels in two cases and postprandial serum bile acid level in one case were normal. Light microscopic findings of the liver revealed normal histology. Electron microscopic findings showed increase of lipofuscin-like lysosomes, modification and paracrystalline-like array of mitochondria, and an increase of reticulum fiber in Disse's space. It is suggested that these cases represent a new type of dye excretory disorder of the liver with impaired hepatic uptake of ICG.

摘要

9例患者吲哚菁绿(ICG)试验显示明显潴留,而磺溴酞钠(BSP)试验正常。除ICG试验外,这些病例的肝功能检查结果均在正常范围内。ICG血浆消失率为0.017至0.025,而BSP的血浆消失率为0.058至0.126。对ICG衰变曲线进行二室分析时,ICG从血浆向肝脏的转运率明显降低。在重复观察后,所有病例在注射后20至25分钟内,ICG衰变曲线上均观察到ICG血浆消失的短暂延迟(阶梯形成)。这些病例中ICG与血浆蛋白的结合与正常受试者相比无显著差异。2例患者的空腹血清胆汁酸水平及1例患者的餐后血清胆汁酸水平均正常。肝脏的光镜检查结果显示组织学正常。电镜检查结果显示脂褐素样溶酶体增多、线粒体形态改变及类副晶样排列,狄氏间隙内网状纤维增多。提示这些病例代表一种新型的肝脏染料排泄障碍,伴有ICG肝脏摄取受损。

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1
Nine cases with marked retention of indocyanine green test and normal sulfobromophthalein test without abnormal liver histology: constitutional indocyanine green excretory defect.9例吲哚菁绿试验明显潴留且磺溴酞钠试验正常,肝脏组织学无异常:体质性吲哚菁绿排泄缺陷。
Hepatogastroenterology. 1981 Feb;28(1):6-12.
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引用本文的文献

1
Physiologically Based Modeling of the Effect of Physiological and Anthropometric Variability on Indocyanine Green Based Liver Function Tests.基于生理和人体测量变异性对基于吲哚菁绿的肝功能测试影响的生理模型。
Front Physiol. 2021 Nov 22;12:757293. doi: 10.3389/fphys.2021.757293. eCollection 2021.
2
Impaired lesion detectability on gadoxetic acid-enhanced MR imaging in indocyanine green excretory defect: case series of three patients.钆塞酸增强磁共振成像中吲哚菁绿排泄缺陷时病灶检出能力受损:三例病例系列。
Jpn J Radiol. 2020 Oct;38(10):997-1003. doi: 10.1007/s11604-020-00991-9. Epub 2020 May 27.
3
Hepatectomy in a case of hepatocellular carcinoma with constitutional indocyanine green excretory defect.
1例伴有体质性吲哚菁绿排泄缺陷的肝细胞癌患者的肝切除术
Int J Surg Case Rep. 2018;53:231-234. doi: 10.1016/j.ijscr.2018.10.074. Epub 2018 Nov 1.
4
Loss of organic anion transporting polypeptide 1B3 function causes marked delay in indocyanine green clearance without any clinical symptoms.有机阴离子转运多肽1B3功能丧失会导致吲哚菁绿清除明显延迟,且无任何临床症状。
Hepatology. 2017 Mar;65(3):1065-1068. doi: 10.1002/hep.28950. Epub 2017 Jan 6.
5
Hepatic transport of serum bilirubin, bromsulfophthalein, and indocyanine green in patients with congenital non-hemolytic hyperbilirubinemia and patients with constitutional indocyanine green excretory defect.先天性非溶血性高胆红素血症患者及体质性吲哚菁绿排泄缺陷患者血清胆红素、磺溴酞钠和吲哚菁绿的肝脏转运
J Gastroenterol. 1996 Apr;31(2):228-36. doi: 10.1007/BF02389522.
6
Hepatic transport and metabolism of various organic anions in patients with congenital non-hemolytic hyperbilirubinemia, including constitutional indocyanine green excretory defect.先天性非溶血性高胆红素血症患者中各种有机阴离子的肝脏转运和代谢,包括体质性吲哚菁绿排泄缺陷。
J Gastroenterol. 1994 Apr;29(2):228-40. doi: 10.1007/BF02358689.
7
Studies on the pathogenesis of the constitutional excretory defect of indocyanine green.吲哚菁绿体质性排泄缺陷的发病机制研究。
Gastroenterol Jpn. 1982;17(4):301-9. doi: 10.1007/BF02774575.