Department of Pathology, Medical College of Georgia, Augusta, USA.
Ann Diagn Pathol. 2011 Oct;15(5):323-8. doi: 10.1016/j.anndiagpath.2011.02.010. Epub 2011 Jun 8.
Historically, the diagnosis of Hirschsprung disease was made by evaluating multiple hematoxylin and eosin-stained slides and performing acetylcholinesterase histochemical staining. Recently, calretinin immunohistochemical staining has been reported and found to be superior to acetylcholinesterase staining in the confirmation of aganglionosis. We retrieved tissue blocks from 23 patients with proven Hirschsprung disease from the archives of the Medical College of Georgia. In addition, we selected 23 control patients with ganglion cells. All cases were stained with calretinin, and the presence or absence of both intrinsic nerve fibers (INFs) and ganglion cells was scored by 4 pathologists with fairly strong agreement (κ = 0.858). All cases of proven Hirschsprung disease were negative for INFs. Eighty-three percent of non-Hirschsprung patients were positive for INFs. Based on statistical analysis, the association between disease status and pathologist rating was statistically significant (P < .0001). We also found calretinin immunostaining to be a useful adjunctive modality in the diagnosis of Hirschsprung disease.
从历史上看,先天性巨结肠的诊断是通过评估多个苏木精和曙红染色的幻灯片,并进行乙酰胆碱酯酶组织化学染色来完成的。最近,钙视网膜蛋白免疫组织化学染色已被报道,并被发现优于乙酰胆碱酯酶染色,可用于确认无神经节细胞病变。我们从佐治亚医学院的档案中检索了 23 例经证实的先天性巨结肠患者的组织块。此外,我们选择了 23 例有神经节细胞的对照患者。所有病例均用钙视网膜蛋白染色,4 位病理学家对内在神经纤维(INFs)和神经节细胞的存在或缺失进行评分,具有相当强的一致性(κ=0.858)。所有经证实的先天性巨结肠病例均无 INFs。83%的非先天性巨结肠患者的 INFs 阳性。基于统计学分析,疾病状态与病理学家评分之间的关联具有统计学意义(P<0.0001)。我们还发现钙视网膜蛋白免疫染色是诊断先天性巨结肠的一种有用的辅助方法。