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先天性巨结肠症治疗的最新进展

Recent advances in the management of Hirschsprung's disease.

作者信息

Coran A G, Teitelbaum D H

机构信息

Department of Surgery, Section of Pediatric Surgery, University of Michigan Medical School, and the C. S. Mott Children's Hospital, Ann Arbor, Michigan 48109-0245, USA.

出版信息

Am J Surg. 2000 Nov;180(5):382-7. doi: 10.1016/s0002-9610(00)00487-6.

Abstract

BACKGROUND

Major advances have occurred in the management of Hirschsprung's disease since Swenson described his definitive operation in 1948. These advances have occurred in the following areas: genetics, neurophysiology, definitive management in the newborn, total colonic aganglionosis (TCA), Hirschsprung's-associated enterocolitis (HAEC), intestinal neuronal dysplasia (IND), and laparoscopic and perineal approaches for definitive pull-through and redo pull-through operations.

METHODS

This paper will focus on the definitive management of the newborn, TCA, and HAEC, areas in which we have had considerable experience at our institution.

RESULTS

We have treated almost 90 newborns with the definitive pull-through with minimum morbidity. We have managed 25 patients with TCA, of whom 5 had total intestinal involvement and died. The remaining 20 have undergone a total colectomy and endorectal pull-through (ERPT), with zero mortality and a very acceptable stooling pattern and continence rate. Our experience with more than 350 patients with Hirschsprung's disease over the past 25 years has demonstrated an incidence of HAEC of between 20% and 30%. During this period, we have performed 19 redo pull-through operations, the majority of which were ERPTs, with results comparable with those seen with a primary pull-through operation.

CONCLUSIONS

The major advances that have occurred in the management of Hirschsprung's disease include the definitive management of the newborn, our understanding of Hirschsprung's-associated enterocolitis and the treatment of this entity, and the recent successful management of the very complex form of this disease, total colonic aganglionosis.

摘要

背景

自1948年斯文森描述其根治性手术以来,先天性巨结肠症的治疗取得了重大进展。这些进展体现在以下几个方面:遗传学、神经生理学、新生儿的根治性治疗、全结肠无神经节细胞症(TCA)、先天性巨结肠相关小肠结肠炎(HAEC)、肠道神经元发育异常(IND),以及根治性拖出术和再次拖出术的腹腔镜和会阴入路。

方法

本文将重点关注新生儿的根治性治疗、TCA和HAEC,这些是我们机构有丰富经验的领域。

结果

我们已用根治性拖出术治疗了近90例新生儿,发病率极低。我们治疗了25例TCA患者,其中5例全肠道受累并死亡。其余20例接受了全结肠切除术和直肠内拖出术(ERPT),死亡率为零,排便模式和控便率非常理想。在过去25年里,我们对350多名先天性巨结肠症患者的治疗经验表明,HAEC的发病率在20%至30%之间。在此期间,我们进行了19例再次拖出术,其中大多数是ERPT,结果与初次拖出术相当。

结论

先天性巨结肠症治疗方面的主要进展包括新生儿的根治性治疗、我们对先天性巨结肠相关小肠结肠炎的认识及对该病症的治疗,以及最近对这种疾病非常复杂的形式——全结肠无神经节细胞症的成功治疗。

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