• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

先天性巨结肠症和肠神经元发育不良的肠神经系统免疫组织化学研究。

Immunohistochemical study of enteric nervous system in hirschsprung's disease and intestinal neuronal dysplasia.

机构信息

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Histol Histopathol. 2013 Mar;28(3):345-51. doi: 10.14670/HH-28.345.

DOI:10.14670/HH-28.345
PMID:23348388
Abstract

BACKGROUND

Hirschsprung's disease (HD) is one of the most common motility disorders in pediatric age groups and it is very important that it be differentiated from other types of motility disorders, especially intestinal neuronal dysplasia B (IND B). Although many studies regarding the differences between the two disorders by immunohistochemical studies exist, there is as yet no consistent result. The purpose of this research was to study the immunohistochemical findings of enteric nervous system in these two motility disorders in comparison with colectomies without motility disorder.

METHODS

Full wall thickness specimens of three groups of patients (HD, IND B and non motility disorders) were included in the study to be evaluated by immunohistochemistry (IHC). Markers were specific for neuronal cells and pace maker cells composed of PGP 9.5, c-kit, synaptophysin, S100 and CD56. The number of cells was evaluated in the muscularis properia, and myenteric plexus.

RESULTS

The number of all the IHC markers i.e. PGP9.5, c-kit, synaptophysin, S100 and CD56 was completely different in HD from the two other groups, while IND B was quite similar to control group.

CONCLUSION

Our finding suggests that there is a marked and significant difference between HD and IND B by IHC markers, which can be used as an additional test for the diagnosis of HD with more accuracy. Further multicenter studies with a greater number of cases would be necessary to find a cut-off point for every IHC marker to differentiate HD and IND B.

摘要

背景

先天性巨结肠(HD)是小儿时期最常见的动力障碍之一,将其与其他类型的动力障碍(尤其是肠神经元发育不良 B 型,IND B)区分开来非常重要。尽管有许多关于两种疾病通过免疫组织化学研究的差异的研究,但目前还没有一致的结果。本研究旨在通过免疫组织化学研究,比较这两种动力障碍与无动力障碍的结肠切除术,研究肠神经系统的免疫组织化学发现。

方法

本研究纳入了三组患者(HD、IND B 和非动力障碍)的全壁厚度标本,通过免疫组织化学(IHC)进行评估。标记物是针对神经元细胞和起搏细胞的,由 PGP 9.5、c-kit、突触素、S100 和 CD56 组成。在固有肌层和肌间神经丛中评估细胞数量。

结果

所有免疫组织化学标志物(PGP9.5、c-kit、突触素、S100 和 CD56)在 HD 组与其他两组之间的数量完全不同,而 IND B 与对照组非常相似。

结论

我们的发现表明,HD 和 IND B 之间存在明显而显著的差异,这些差异可以作为诊断 HD 的附加测试,以提高诊断的准确性。需要进行更多的多中心研究,并纳入更多的病例,以找到每个免疫组织化学标志物的截止值,从而区分 HD 和 IND B。

相似文献

1
Immunohistochemical study of enteric nervous system in hirschsprung's disease and intestinal neuronal dysplasia.先天性巨结肠症和肠神经元发育不良的肠神经系统免疫组织化学研究。
Histol Histopathol. 2013 Mar;28(3):345-51. doi: 10.14670/HH-28.345.
2
Immunohistochemical studies of pediatric intestinal pseudo-obstruction: bcl2, a valuable biomarker to detect immature enteric ganglion cells.小儿肠道假性梗阻的免疫组织化学研究:bcl2,一种检测未成熟肠神经节细胞的重要生物标志物。
Am J Surg Pathol. 2005 Aug;29(8):1017-24.
3
Interstitial cells of Cajal reduce in number in recto-sigmoid Hirschsprung's disease and total colonic aganglionosis.在直肠乙状结肠型先天性巨结肠症和全结肠无神经节细胞症中,Cajal间质细胞数量减少。
Neurosci Lett. 2009 Feb 27;451(3):208-11. doi: 10.1016/j.neulet.2009.01.015. Epub 2009 Jan 13.
4
Evaluation of PGP9.5 in the diagnosis of Hirschsprung's disease.PGP9.5在先天性巨结肠症诊断中的评估
J Pathol. 1992 Sep;168(1):55-8. doi: 10.1002/path.1711680110.
5
Histological studies on Hirschsprung's disease and its allied disorders in childhood.儿童先天性巨结肠及其相关疾病的组织学研究。
Hepatogastroenterology. 2004 Jul-Aug;51(58):1042-4.
6
An abnormal distribution of C-kit positive cells in the normoganglionic segment can predict a poor clinical outcome in patients with Hirschsprung's disease.在无神经节段中C-kit阳性细胞的异常分布可预测先天性巨结肠症患者的临床预后不良。
Eur J Pediatr Surg. 2005 Jun;15(3):153-8. doi: 10.1055/s-2005-837612.
7
The expression of enteric nerve markers and nerve innervation in total colonic aganglionosis.全结肠无神经节症中肠神经标志物的表达及神经支配情况
Int J Surg Pathol. 2011 Jun;19(3):303-8. doi: 10.1177/1066896910361738. Epub 2010 Jul 18.
8
PTEN Immunohistochemistry.PTEN 免疫组化。
Arch Pathol Lab Med. 2022 May 1;147(5):577-583. doi: 10.5858/arpa.2021-0424-OA.
9
Enteric nervous system impairment in gastroschisis.腹裂患儿的肠神经系统损伤
Eur J Pediatr Surg. 2013 Feb;23(1):29-38. doi: 10.1055/s-0032-1326955. Epub 2012 Oct 25.
10
Is intestinal neuronal dysplasia a disorder of the neuromuscular junction?肠道神经元发育异常是神经肌肉接头的一种疾病吗?
J Pediatr Surg. 1996 Apr;31(4):575-9. doi: 10.1016/s0022-3468(96)90500-x.

引用本文的文献

1
A combinatorial panel for flow cytometry-based isolation of enteric nervous system cells from human intestine.一种基于流式细胞术的组合面板,用于从人肠道中分离肠神经细胞。
EMBO Rep. 2023 Apr 5;24(4):e55789. doi: 10.15252/embr.202255789. Epub 2023 Feb 28.
2
Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells.肠神经元发育不良 B 型的诊断挑战:超越神经节细胞数量的观察。
World J Gastroenterol. 2021 Nov 28;27(44):7649-7660. doi: 10.3748/wjg.v27.i44.7649.
3
The maintenance of adult peripheral adult nerve and microvascular networks in the rat mesentery culture model.
大鼠肠系膜培养模型中成年外周神经和微血管网络的维持
J Neurosci Methods. 2020 Dec 1;346:108923. doi: 10.1016/j.jneumeth.2020.108923. Epub 2020 Sep 1.
4
Laparoscopic-assisted endorectal pull-through for Hirschsprung's disease. A retrospective study.腹腔镜辅助经肛门直肠拖出术治疗先天性巨结肠:一项回顾性研究。
Saudi Med J. 2017 Dec;38(12):1255-1258. doi: 10.15537/smj.2017.12.20859.
5
Immunostaining for Hu C/D and CD56 is useful for a definitive histopathological diagnosis of congenital and acquired isolated hypoganglionosis.Hu C/D和CD56免疫染色有助于先天性和后天性孤立性神经节减少症的确切组织病理学诊断。
Virchows Arch. 2017 Jun;470(6):679-685. doi: 10.1007/s00428-017-2128-9. Epub 2017 Apr 19.
6
A critical appraisal of the morphological criteria for diagnosing intestinal neuronal dysplasia type B.B 型肠神经元发育不良形态学诊断标准的批判性评价。
Mod Pathol. 2017 Jul;30(7):978-985. doi: 10.1038/modpathol.2017.4. Epub 2017 Mar 17.
7
Global hypoxia-ischemia induced inflammation and structural changes in the preterm ovine gut which were not ameliorated by mesenchymal stem cell treatment.全球缺氧缺血诱导早产羊肠道发生炎症和结构变化,间充质干细胞治疗并未改善这些变化。
Mol Med. 2016 Sep;22:244-257. doi: 10.2119/molmed.2015.00252. Epub 2016 Apr 14.
8
Evaluation of Calretinin as a New Marker in the Diagnosis of Hirschsprung Disease.评估钙视网膜蛋白作为先天性巨结肠症诊断新标志物的作用。
Iran J Pediatr. 2015 Apr;25(2):e367. doi: 10.5812/ijp.367. Epub 2015 Apr 18.
9
Interstitial cells of Cajal in the normal human gut and in Hirschsprung disease.正常人类肠道和先天性巨结肠中的 Cajal 间质细胞。
Pediatr Surg Int. 2013 Sep;29(9):889-97. doi: 10.1007/s00383-013-3364-y.