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小肠移植急性细胞排斥反应的国际分级方案:单中心经验

International grading scheme for acute cellular rejection in small-bowel transplantation: single-center experience.

作者信息

Ruiz P, Takahashi H, Delacruz V, Island E, Selvaggi G, Nishida S, Moon J, Smith L, Asaoka T, Levi D, Tekin A, Tzakis A G

机构信息

Department of Surgery, University of Miami School of Medicine, Miami, FL, USA.

出版信息

Transplant Proc. 2010 Jan-Feb;42(1):47-53. doi: 10.1016/j.transproceed.2009.12.026.

Abstract

A standardized grading scheme for the assessment of acute cellular rejection (ACR) in small-intestine transplantation was proposed in 2003 at the Eighth International Small Intestinal Transplantation Symposium. We have implemented the current grading scheme for ACR in small-bowel transplantation since October 2003. The pathologic diagnoses of those small-intestine biopsy samples, including ACR grade and other supplementary findings were evaluated. A total of 3484 small intestine biopsy samples from 155 patients were available for evaluation in this study. Frequency of grades 0, indeterminate, 1, 2, and 3 acute cellular rejection was 33.9%, 49.1%, 12.6%, 3.7%, and 0.8%, respectively. Duration of ACR episode strongly correlated with grade of ACR episode (P < .001). Other supplementary findings included acute vascular rejection component, 2.2%; increase in lymphoplasmacytic infiltrate in lamina propria, 15.7%; mucosal fibrosis, 0.4%; and regenerative changes, 0.3%. Our data substantiate that this grading system is reliable and useful for clinical decision making in bowel transplantation. We suggest that an assessment and quantification of supplementary findings be considered a component of the International Pathology Grading Scheme.

摘要

2003年第八届国际小肠移植研讨会上提出了一种用于评估小肠移植中急性细胞排斥反应(ACR)的标准化分级方案。自2003年10月起,我们在小肠移植中实施了当前的ACR分级方案。对那些小肠活检样本的病理诊断进行了评估,包括ACR分级和其他补充发现。本研究共纳入了155例患者的3484份小肠活检样本进行评估。0级、不确定级、1级、2级和3级急性细胞排斥反应的发生率分别为33.9%、49.1%、12.6%、3.7%和0.8%。ACR发作的持续时间与ACR发作的分级密切相关(P <.001)。其他补充发现包括急性血管排斥成分,占2.2%;固有层淋巴浆细胞浸润增加,占15.7%;黏膜纤维化,占0.4%;以及再生性改变,占0.3%。我们的数据证实,该分级系统对于肠道移植的临床决策是可靠且有用的。我们建议将补充发现的评估和量化视为国际病理分级方案的一个组成部分。

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