Kinra P, Turlapati Spv, Mehta A, Rai Ramji
Graded Specialist (Pathology), 7 Air Force Hospital, Kanpur-4.
Classified Specialist (Pathology), Military Hospital Allahabad.
Med J Armed Forces India. 2005 Feb;61(2):125-9. doi: 10.1016/S0377-1237(05)80006-1. Epub 2011 Jul 21.
Dysplasia in ulcerative colitis has been graded on haematoxylin and eosin stain using Riddle's criteria. This system was formed to nullify the inter-observer variation. Few cases of early dysplasia were missed when purely screened on morphology. This study was carried out to detect early dysplasia using p53 and bcl-2 oncoproteins.
A retrospective study was carried out on paraffin blocks of 100 histologically diagnosed cases of ulcerative colitis at a large service hospital. Haematoxylin and Eosin stained (H &E) slides of these cases were re-examined as per standard techniques.
On correlating histological grades with p53 immunoscore it was found that 90.76% of cases graded as negative for dysplasia on H & E, got an immunoscore of 0 and other 9.24% cases which were graded as negative for dysplasia got a score 1+. This shows that the immunohistochemistry was able to pick up 6 cases, which were missed by routine histology. Nine out of 11 cases in which the pathologists could not rule out a dysplasia and graded them as indefinite (probably negative for dysplasia) got a score of 0. In these cases possibly the histological features may be construed as an acute inflammation or repair induced dysplasia which were suspicious for neoplastic dysplasia on routine histology sections. On analyzing our findings on bcl-2 immunohistochemistry it was seen that there was no significant concordance (p>0.05) of immunoscore with the grades of dysplasia estimated morphologically.
Our study recommends that p53 should be used as regular immunohistochemical marker while grading the dysplasia of ulcerative colitis, especially in indefinite cases as it brings objectivity in grading. Our study also came to a conclusion that use of bcl-2 for grading dysplasia of ulcerative colitis is not of any significant help.
溃疡性结肠炎的发育异常已根据里德尔标准通过苏木精和伊红染色进行分级。该系统的形成是为了消除观察者之间的差异。单纯从形态学上筛查时,很少有早期发育异常的病例被漏诊。本研究旨在利用p53和bcl-2癌蛋白检测早期发育异常。
在一家大型服务医院对100例经组织学诊断的溃疡性结肠炎石蜡块进行回顾性研究。按照标准技术对这些病例的苏木精和伊红染色(H&E)切片进行重新检查。
将组织学分级与p53免疫评分相关联后发现,在H&E染色中被分级为发育异常阴性的病例中,90.76%的免疫评分为0,其他9.24%被分级为发育异常阴性的病例免疫评分为1+。这表明免疫组化能够检出6例常规组织学漏诊的病例。在11例病理学家无法排除发育异常并将其分级为不确定(可能为发育异常阴性)的病例中,有9例评分为0。在这些病例中,组织学特征可能被解释为急性炎症或修复性发育异常,在常规组织学切片上怀疑为肿瘤性发育异常。分析我们关于bcl-2免疫组化的结果发现,免疫评分与形态学评估的发育异常分级之间没有显著一致性(p>0.05)。
我们的研究建议,在对溃疡性结肠炎的发育异常进行分级时,应将p53用作常规免疫组化标记物,尤其是在不确定的病例中,因为它能使分级更客观。我们的研究还得出结论,使用bcl-2对溃疡性结肠炎的发育异常进行分级没有任何显著帮助。