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先天性巨结肠

Hirschsprung disease.

作者信息

Haricharan Ramanath N, Georgeson Keith E

机构信息

Division of Pediatric Surgery, Department of General Surgery, University of Alabama at Birmingham, Birmingham, Alabama 35233, USA.

出版信息

Semin Pediatr Surg. 2008 Nov;17(4):266-75. doi: 10.1053/j.sempedsurg.2008.07.005.

DOI:10.1053/j.sempedsurg.2008.07.005
PMID:19019295
Abstract

Hirschsprung disease is a relatively common condition managed by pediatric surgeons. Significant advances have been made in understanding its etiologies in the last decade, especially with the explosion of molecular genetic techniques and early diagnosis. The surgical management has progressed from a two- or three-stage procedure to a primary operation. More recently, definitive surgery for Hirschsprung disease through minimally invasive techniques has gained popularity. In neonates, the advancement of treatment strategies for Hirschsprung disease continues with reduced patient morbidity and improved outcomes.

摘要

先天性巨结肠症是一种由小儿外科医生治疗的相对常见的病症。在过去十年中,对其病因的理解取得了重大进展,尤其是随着分子遗传学技术的迅猛发展和早期诊断技术的进步。手术治疗已从两阶段或三阶段手术发展为一期手术。最近,通过微创技术进行先天性巨结肠症的确定性手术越来越受欢迎。在新生儿中,先天性巨结肠症的治疗策略不断进步,患者发病率降低,治疗效果得到改善。

相似文献

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Hirschsprung disease.先天性巨结肠
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Large bowel obstruction in an adult after Soave for Hirschsprung's disease in childhood.儿童期行Soave手术治疗先天性巨结肠症后成人发生的大肠梗阻。
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[Congenital megacolon in neonates and infants: impact of early, one-stage repair on morbidity and surgical complications].[新生儿及婴儿先天性巨结肠:早期一期修复对发病率及手术并发症的影响]
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引用本文的文献

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Single-cell RNA sequencing in Hirschsprung's disease tissues reveals lack of neuronal differentiation in the aganglionic colon segment.先天性巨结肠组织的单细胞RNA测序揭示了无神经节结肠段中神经元分化的缺乏。
bioRxiv. 2025 Jul 4:2025.07.01.662516. doi: 10.1101/2025.07.01.662516.
2
Atypical Presentation of Hirschsprung's Disease in an Infant: Challenges in Early Diagnosis and Management of Recurrent Enterocolitis.婴儿先天性巨结肠的非典型表现:复发性小肠结肠炎早期诊断与管理中的挑战
Cureus. 2024 Nov 17;16(11):e73862. doi: 10.7759/cureus.73862. eCollection 2024 Nov.
3
Evaluation of Trans-Anal Endorectal Pull-Through Outcomes in Hirschsprung's Disease in Different Age Groups: A Comprehensive Systematic Review.
不同年龄段先天性巨结肠经肛门直肠内拖出术治疗效果的评估:一项全面的系统性综述。
Arch Iran Med. 2024 Jul 1;27(7):392-399. doi: 10.34172/aim.28183.
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Early Detection and Intervention for Hirschsprung's Disease: A Key to Successful Outcomes.先天性巨结肠症的早期检测与干预:成功治疗的关键
Clin Med Insights Case Rep. 2024 Jan 23;17:11795476241226577. doi: 10.1177/11795476241226577. eCollection 2024.
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Postoperative Hirschsprung's associated enterocolitis (HAEC): transition zone as putative histopathological predictive factor.术后先天性巨结肠相关小肠结肠炎(HAEC):过渡区作为假定的组织病理学预测因素。
J Clin Pathol. 2025 Jan 17;78(2):111-116. doi: 10.1136/jcp-2023-209129.
6
State of the Art Bowel Management for Pediatric Colorectal Problems: Hirschsprung Disease.小儿结直肠问题的最新肠道管理:先天性巨结肠症
Children (Basel). 2023 Aug 20;10(8):1418. doi: 10.3390/children10081418.
7
Comparison between two minimally invasive techniques for Hirschsprung disease: transanal endorectal pull-through (TERPT) versus laparoscopic-TERPT.两种微创技术治疗先天性巨结肠的比较:经肛门内拖出术(TERPT)与腹腔镜-TERPT。
Pediatr Surg Int. 2023 May 13;39(1):198. doi: 10.1007/s00383-023-05473-3.
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Identifying the potential transcriptional regulatory network in Hirschsprung disease by integrated analysis of microarray datasets.通过微阵列数据集的综合分析鉴定先天性巨结肠症潜在的转录调控网络。
World J Pediatr Surg. 2023 Apr 17;6(2):e000547. doi: 10.1136/wjps-2022-000547. eCollection 2023.
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Functional outcome of Hirschsprung's disease in children: A single center study at The Children's Hospital Lahore.先天性巨结肠患儿的功能预后:拉合尔儿童医院的单中心研究。
Pediatr Surg Int. 2023 Apr 11;39(1):176. doi: 10.1007/s00383-023-05451-9.
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The utility of the 24-h delayed film of barium enema for detecting the dysganglionic bowel segment in Hirschsprung's disease.钡剂灌肠24小时延迟片在检测先天性巨结肠症无神经节肠段中的应用。
Front Pediatr. 2022 Sep 20;10:979149. doi: 10.3389/fped.2022.979149. eCollection 2022.