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先天性巨结肠全结肠无神经节细胞症。

Total Colonic Aganglionosis in Hirschsprung disease.

机构信息

Department of Pediatric Colorectal and Pelvic Reconstructive Surgery, Nationwide Children's Hospital, Columbus, OH, USA.

Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

出版信息

Semin Pediatr Surg. 2022 Apr;31(2):151165. doi: 10.1016/j.sempedsurg.2022.151165. Epub 2022 Apr 20.

DOI:10.1016/j.sempedsurg.2022.151165
PMID:35690465
Abstract

Total Colonic Hirschsprung Disease (HD) can be challenging from a diagnostic and management standpoint and occurs in around 8% of cases of HD. Long term outcomes are difficult to compare due to variation in length of aganglionosis, chosen surgical techniques, and terminology utilized in the literature. In this review we highlight some of the management controversies and clinical challenges and emphasize future areas of suggested collaboration and research.

摘要

全结肠型先天性巨结肠(HD)在诊断和治疗方面具有挑战性,约占 HD 病例的 8%。由于无神经节细胞的长度、选择的手术技术以及文献中使用的术语存在差异,长期预后难以比较。在这篇综述中,我们强调了一些治疗争议和临床挑战,并强调了未来建议合作和研究的领域。

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1
Total Colonic Aganglionosis in Hirschsprung disease.先天性巨结肠全结肠无神经节细胞症。
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Risk factors and simple scoring system for predicting postoperative nutritional status of Hirschsprung's disease.预测先天性巨结肠症术后营养状况的危险因素及简易评分系统
Front Nutr. 2024 Dec 6;11:1441104. doi: 10.3389/fnut.2024.1441104. eCollection 2024.
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