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Interobserver study on histologic features of idiopathic non-cirrhotic portal hypertension

机译:Interobserver关于特发性非肝硬化门户高血压的组织学特征的研究

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Abstract Background Histologic features of idiopathic non-cirrhotic portal hypertension (INCPH) may overlap with those without INCPH. Recently, these features have been recognized as part of the larger spectrum of porto-sinusoidal vascular disease (PSVD). We assessed interobserver agreement on histologic features that are commonly associated with INCPH and studied whether a provision of relevant clinical history improves interobserver agreement. Methods The examined histologic features include lobular (such as anisocytosis, nodular regeneration, sinusoidal dilatation, increased parenchymal draining veins, and incomplete fibrous septa) and portal tract changes (such as paraportal shunting vessel(s), portal tract remnant, increased number of portal vessels, and obliterative portal venopathy). Thirty-four archived liver samples from patients with (group A) and without (group B) INCPH were retrieved. A total of 90 representative images of lobules (L) and portal tracts (P) were distributed among 9 liver pathologists blinded to true clinical history. Each pathologist answered multiple choice questions based on the absence (Q1) or presence (Q2) of clinical history of portal hypertension. Fleiss’ kappa coefficient analysis (unweighted) was performed to assess interobserver agreement on normal versus abnormal diagnosis, in L and P, based on Q1 and Q2. Results The kappa values regarding normal versus abnormal diagnosis were 0.24, 0.24, 0.18 and 0.18 for L-Q1, L-Q2, P-Q1, and P-Q2, respectively. With true clinical history provided, the kappa values were L- 0.32, P-0.17 for group A and L-0.12, P-0.14 for group B. Four pathologists changed their assessments based on the provided history. Interobserver agreement on the interpretation of L and P as normal versus abnormal was slight to fair regardless of provision of clinical history. Conclusions Our findings indicate that the histologic features of INCPH/PSVD are not limited to patients with portal hypertension and are subject to significant interobserver variation.
机译:摘要特发性非肝硬化门静脉高压(​​INCPH)的背景技术组织特征可能与没有INCPH的人重叠。最近,这些特征被认为是较大光谱的波多族血管血管疾病(PSVD)的一部分。我们评估了Interobserver协议关于与Incph共同关联的组织学功能,并研究了相关的临床历史是否改善了Interobserver协议。方法,所检测的组织学特征包括小叶(如胞虫病,结节性再生,正弦扩张,增加的实质排水静脉和不完全的纤维化静脉)和门户道变化(如帕拉斯特分流容器,门户道残留,门户数量增加。血管和抹败的门静脉病变。检索来自(A组)和没有(B组)INCP的患者的34个存档肝脏样本。共有90个叶片(L)和门龟(P)的代表性图像分布在蒙蔽真正的临床史上的9位肝脏病理学家中。每个病理学家基于门静脉高血压临床病史的缺席(Q1)或存在(Q2)回答了多项选择题。根据Q1和Q2,执行Fleish'Appa系数分析(未加权)以评估正常与异常诊断的Interobserver协议。结果L-Q1,L-Q2,P-Q1和P-Q2的正常诊断的Kappa值分别为0.24,0.24,0.18和0.18。通过提供真正的临床历史,Kappa值为L- 0.32,P-0.17对于A组和B组,B-0.14的P-0.14。四位病理学家根据提供的历史改变了评估。无论提供临床历史如何,Interobserver协议达到L和P的解释与正常相反的略显略有公平。结论我们的研究结果表明,INCPH / PSVD的组织学特征不仅限于门静脉高压患者,并且受到显着的Interobserver变异。

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