首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Smoothelin and caldesmon are reliable markers for distinguishing muscularis propria from desmoplasia: a critical distinction for accurate staging colorectal adenocarcinoma
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Smoothelin and caldesmon are reliable markers for distinguishing muscularis propria from desmoplasia: a critical distinction for accurate staging colorectal adenocarcinoma

机译:Smoothelin和Caldesmon是区分固有肌层和增生的可靠标志物:对准确分期大肠腺癌的关键区别

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摘要

An accurate distinction between deep muscularis propria invasion versus subserosal invasion by colonic adenocarcinoma is essential for the accurate staging of cancer and subsequent optimal patient management. However, problems may arise in pathologic staging when extensive desmoplasia blurs the junction between deep muscularis propria and subserosal fibroadipose tissue. To address this issue, forty-three (43) cases of colonic adenocarcinoma resections from 2007-2009 at The Methodist Hospital in Houston, TX were reviewed. These cases were selected to address possible challenges in differentiating deep muscularis propria invasion from superficial subserosal invasion based on H&E staining alone. Immunohistochemical staining using smooth muscle actin (SMA), smoothelin, and caldesmon were performed on 51 cases: 8 cases of pT1 tumors (used mainly as control); 12 pT2 tumors; and 31 pT3 tumors. All 51 (100%) had diffuse, strong (3+) immunoreactivity for caldesmon and smoothelin in the muscularis propria with a granular cytoplasmic staining pattern. However, the desmoplastic areas of these tumors, composed of spindled fibroblasts and myofibroblasts, showed negative immunostaining for caldesmon and smoothelin (0/35). SMA strongly stained the muscularis propria and weakly (1+) or moderately (2+) stained the spindled fibroblasts in the desmoplastic areas (the latter presumably because of myofibroblastic differentiation). Compared to SMA, caldesmon and smoothelin are more specific stains that allow better delineation of the muscularis propria from the desmoplastic stromal reaction which provides a critical aide for proper staging of colonic adenocarcinoma and subsequent patient care.
机译:结肠腺癌在深部肌层固有层浸润与浆膜下浸润之间的准确区分对于癌症的准确分期和随后的最佳患者管理至关重要。但是,当广泛的异型增生模糊深部固有肌层和浆膜下纤维脂肪组织之间的连接时,病理分期可能会出现问题。为了解决这个问题,回顾了德克萨斯州休斯顿卫理公会医院2007年至2009年的四十三(43)例结肠腺癌切除术。选择这些病例是为了解决仅基于H&E染色将深部肌层浸润与浅表浆膜下浸润区分开的可能挑战。使用平滑肌肌动蛋白(SMA),平滑肌素和caldesmon对51例患者进行了免疫组织化学染色:8例pT1肿瘤(主要用作对照); pT1肿瘤8例。 12个pT2肿瘤;和31个pT3肿瘤。所有51(100%)对固有肌层中的Caldesmon和Smoothelin具有弥散的,强的(3+)免疫反应性,具有颗粒状细胞质染色模式。但是,由梭形成纤维细胞和成肌纤维细胞组成的这些肿瘤的去增塑区对caldesmon和平滑肌素的免疫染色呈阴性(0/35)。 SMA在增生区域强烈染色固有肌层,对纺锤形成纤维细胞染色较弱(1+)或中度(2 +)(后者可能是由于肌成纤维细胞分化)。与SMA相比,caldesmon和smoothelin是更特异性的染色剂,可以更好地从增生基质反应中区分固有肌层,从而为结肠腺癌的正确分期和随后的患者护理提供了关键助手。

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