Evaluation of Calretinin and enumeration of mast cells in rectum tissue biopsies of Hirschsprung and non-Hirschsprung disease in neonate and infant

Rusul A. Abdul Hussein, Sahar A. H. AL-Sharqi, Nada K. Mehdi, A. Joda
{"title":"Evaluation of Calretinin and enumeration of mast cells in rectum tissue biopsies of Hirschsprung and non-Hirschsprung disease in neonate and infant","authors":"Rusul A. Abdul Hussein, Sahar A. H. AL-Sharqi, Nada K. Mehdi, A. Joda","doi":"10.21931/rb/2023.08.04.32","DOIUrl":null,"url":null,"abstract":"The Hirschsprung disease (HD) is a complex genetic congenital condition characterized by the absence of ganglion cells in the myenteric and submucosal plexuses of the colon and rectum, leading to functional intestinal obstruction. A study was conducted from July 2022 to December 2022. The Toluidine blue stain and calretinin immunohistochemistry were applied to 36 cases of neonates and infants who clinically presented with symptoms suspicious of having HD, And the hematological study of cell blood counts test and compared the result of the HD group with the non-HD group and control group. The study showed an increase in mast cell numbers in the rectal biopsy tissue of HD patients compared with non-HD patients using Toluidine blue stain. The Immunohistochemistry for calretinin result displayed 27 (75%) cases as HD, while the remaining 9 (25%) cases were confirmed as non-HD and showed hypertrophied nerve fiber in HD cases. at the same time, the complete blood count result was unrelated to HD. Some worrying maternal risk factors were highlighted during pregnancy were the age of the mother at conception, maternal illness, intake of drugs, type of Childbirth, and number of previous maternal abortions; all of them show a non-significant difference between the HD group and non-HD group, also consanguineous marriage was detected and shows a significant difference between the HD group and non-HD group.\nKeywords: Hirschsprung, Calretinin, Toluidine blue, CBC count","PeriodicalId":9036,"journal":{"name":"Bionatura","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bionatura","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21931/rb/2023.08.04.32","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The Hirschsprung disease (HD) is a complex genetic congenital condition characterized by the absence of ganglion cells in the myenteric and submucosal plexuses of the colon and rectum, leading to functional intestinal obstruction. A study was conducted from July 2022 to December 2022. The Toluidine blue stain and calretinin immunohistochemistry were applied to 36 cases of neonates and infants who clinically presented with symptoms suspicious of having HD, And the hematological study of cell blood counts test and compared the result of the HD group with the non-HD group and control group. The study showed an increase in mast cell numbers in the rectal biopsy tissue of HD patients compared with non-HD patients using Toluidine blue stain. The Immunohistochemistry for calretinin result displayed 27 (75%) cases as HD, while the remaining 9 (25%) cases were confirmed as non-HD and showed hypertrophied nerve fiber in HD cases. at the same time, the complete blood count result was unrelated to HD. Some worrying maternal risk factors were highlighted during pregnancy were the age of the mother at conception, maternal illness, intake of drugs, type of Childbirth, and number of previous maternal abortions; all of them show a non-significant difference between the HD group and non-HD group, also consanguineous marriage was detected and shows a significant difference between the HD group and non-HD group. Keywords: Hirschsprung, Calretinin, Toluidine blue, CBC count
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
评估新生儿和婴儿赫氏和非赫氏普隆病直肠组织活检中的钙凝蛋白和肥大细胞计数
赫氏病(Hirschsprung disease,HD)是一种复杂的遗传性先天性疾病,其特征是结肠和直肠的肠肌丛和粘膜下神经节细胞缺失,从而导致功能性肠梗阻。研究时间为 2022 年 7 月至 2022 年 12 月。研究人员对 36 例临床表现为疑似 HD 症状的新生儿和婴儿进行了甲苯胺蓝染色和钙网蛋白免疫组化,并进行了细胞血细胞计数检测的血液学研究,将 HD 组与非 HD 组和对照组的结果进行了比较。研究显示,与非 HD 患者相比,HD 患者直肠活检组织中的肥大细胞数量增加。钙网蛋白免疫组化结果显示 27 例(75%)为 HD 患者,其余 9 例(25%)确认为非 HD 患者,并显示 HD 患者的神经纤维肥大。妊娠期一些令人担忧的母体危险因素包括母亲受孕年龄、母亲疾病、药物摄入、分娩方式和母亲流产次数;所有这些因素在HD组和非HD组之间均无显著差异,同时还发现近亲结婚现象,并在HD组和非HD组之间显示出显著差异:Hirschsprung,钙网蛋白,甲苯胺蓝,红细胞计数
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Effect of Foliar Application of Alhagi maurorum Extract on Foeniculum vulgare Growth Production and characterization of flavored goat milk gels using zinc and calcium salts Producing functional foods Effect of spraying with silicon, humic acid, and proline on the safflower tolerance (Carthamus tinctorius L.) to salt stress Biological, serological and molecular characterization of Potato virus Y strains isolated from potato (Solanum tuberosum L.) First report of Alternaria alternata associated with spot blotch of barley (Hordeum vulgare) in Iraq.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1