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合并脐膨出和肛门直肠闭锁的梅干腹综合征。

Prune belly syndrome associated with exomphalos and anorectal agenesis.

作者信息

Walker J, Prokurat A I, Irving I M

出版信息

J Pediatr Surg. 1987 Mar;22(3):215-7. doi: 10.1016/s0022-3468(87)80331-7.

Abstract

We have recently treated a child with prune belly syndrome in association with exomphalos and anorectal agenesis. This case raises the total incidence of exomphalos and anorectal agenesis to four and five, respectively, in our series of 13 cases of prune belly syndrome. Our case report lays emphasis on the severe respiratory problems that can complicate surgery in prune belly patients. We also attempt to relate the pattern of anomalies in our series to the controversy surrounding the embryogenesis of prune belly syndrome and suggest that our case material lends support to the concept of prune belly syndrome being due to an early disturbance of mesodermal development in both the abdominal wall and the urinary tract. We also suggest that the reported occurrence of gastroschisis in association with prune belly syndrome adds weight to the unifying theory of the embryogenesis of gastroschisis and exomphalos.

摘要

我们最近治疗了一名患有梅干腹综合征并伴有脐膨出和肛门直肠闭锁的儿童。在我们的13例梅干腹综合征病例系列中,该病例使脐膨出和肛门直肠闭锁的总发病率分别增至4例和5例。我们的病例报告强调了严重的呼吸问题,这些问题会使梅干腹患者的手术复杂化。我们还试图将我们系列中的异常模式与围绕梅干腹综合征胚胎发生的争议联系起来,并表明我们的病例资料支持梅干腹综合征是由于腹壁和泌尿道中胚层发育早期受到干扰这一概念。我们还认为,报道的腹裂与梅干腹综合征相关的情况进一步支持了腹裂和脐膨出胚胎发生的统一理论。

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