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Histology and Glutamine Synthetase Immunoreactivity in Liver Biopsies From Patients With Congestive Heart Failure

机译:充血性心力衰竭患者肝活检组织学和谷氨酰胺合成酶免疫反应性

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Background: Long-standing congestive heart failure can induce a constellation of histopathology changes in the liver that can range from mild sinusoidal dilation to advanced fibrosis and loss of normal perivenular expression of glutamine synthetase (GS). Liver biopsies might be performed to assess the perioperative risk of these patients or to determine the need of synchronous liver transplant. We aimed to assess interobserver agreement in recognizing these liver histologic features in patients undergoing evaluation for heart transplantation and to examine whether immunohistochemistry of GS will aid the diagnosis of cardiac hepatopathy (CH).Methods: Hematoxylin-eosin and trichrome-stained slides from 36 liver biopsies from patients undergoing evaluation for heart transplantation were reviewed by four liver pathologists. Histologic features of CH were reviewed and an overall fibrosis (stage) was assessed according to a recently proposed congestive hepatic fibrosis score (CHFS). In addition, 24 liver biopsies with a consensus diagnosis of CH and eight liver biopsies with no significant pathological changes were subjected to immunohistochemistry for GS. The Fleiss’ kappa coefficient (K) analysis was performed to determine the interobserver agreement. Further, histologic features of CH were correlated with the staining pattern of GS.Results: Sinusoidal dilation, centrilobular hepatocyte atrophy, centrilobular fibrosis and hemorrhage were the most common findings in this cohort with a substantial-to-fair level of interobserver agreement among four reviewers. The overall agreement on the diagnosis of CH and CHFS was moderate (K = 0.55, 95% confidence interval (CI): 0.32 - 0.73) and fair (K = 0.35, 95% CI: 0.24 - 0.49), respectively. Twelve (of 24, 50%) cases of CH showed loss of the normal perivenular GS staining, while the remaining 12 cases of CH and all eight controls showed retained GS expression. Histologic features of CH (presence of sinusoidal dilation, centrilobular hepatocyte atrophy, hemorrhage, and centrilobular fibrosis) and the stage of fibrosis (CHFS) were not correlated with the loss of GS staining.Conclusion: Most common features of CH can be interpreted with fair-to-substantial level of agreement by liver pathologists, with an overall moderate level agreement for the diagnosis and fair agreement for CHFS. Loss of normal perivenular expression of GS only occurs in 50% CH and thus is not a sensitive marker for CH.Gastroenterol Res. 2017;10(3):182-189doi: https://doi.org/10.14740/gr875e
机译:背景:长期的充血性心力衰竭可引起肝脏组织病理学改变,其范围从轻度正弦波扩张到晚期纤维化以及谷氨酰胺合成酶(GS)的正常静脉周围表达丧失。可能需要进行肝活检以评估这些患者的围手术期风险或确定是否需要同步肝移植。我们的目的是评估观察者之间的共识,以识别接受心脏移植评估的患者的这些肝脏组织学特征,并检查GS的免疫组织化学是否有助于诊断心脏肝病(CH)。方法:苏木精-曙红和三色染色的36片肝脏载玻片四名肝脏病理学家对接受心脏移植评估的患者的活检进行了审查。根据最近提出的充血性肝纤维化评分(CHFS),对CH的组织学特征进行了回顾,并评估了整体纤维化(阶段)。此外,对24例诊断为CH的肝活检和8例无明显病理改变的肝活检进行了GS免疫组织化学检查。进行了Fleiss的kappa系数(K)分析,以确定观察者之间的一致性。此外,CH的组织学特征与GS的染色模式相关。结果:正弦窦扩张,小叶性肝细胞萎缩,小叶性纤维化和出血是该队列中最常见的发现,四位评价者之间观察者之间的同意程度基本相同。 CH和CHFS诊断的总体共识分别为中度(K = 0.55,95%置信区间(CI):0.32-0.73)和一般(K = 0.35,95%CI:0.24-0.49)。 12例(占24%,50%)CH患者丧失了正常的静脉周围GS染色,而其余12例CH患者和所有8例对照均保留了GS表达。 CH的组织学特征(正弦波扩张,小叶性肝细胞萎缩,出血和小叶性纤维化的发生)和纤维化的阶段(CHFS)与GS染色的消失无关。结论:CH的大多数常见特征可以用公平的解释-肝脏病理学家达成的基本同意水平,其中CHFS的诊断总体水平与中等水平一致。 GS的正常静脉周围表达丧失仅发生在50%的CH中,因此不是CH.Gastroenterol Res的敏感标记。 2017; 10(3):182-189doi:https://doi.org/10.14740/gr875e

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