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先天性巨结肠症早期出现首次胎粪排出:一项诊断挑战。

Early presentation of Hirschsprung's disease with initial meconium passage: A diagnostic challenge.

作者信息

Chaudry Tuba, Flesher Susan

机构信息

Department of Pediatrics, Joan C. Edwards Marshall University School of Medicine, Huntington, WV, USA.

出版信息

SAGE Open Med Case Rep. 2025 Jul 29;13:2050313X251360184. doi: 10.1177/2050313X251360184. eCollection 2025.

Abstract

Hirschsprung's disease is a congenital condition characterized by an absence of enteric ganglionic cells. In this paper, we report a case of an 8-day-old male infant presenting with a history of constipation and progressive abdominal distension. Meconium had been passed in the newborn nursery. No stools were passed after 4 days of age, and the last one had required rectal stimulation. We emphasize the diagnostic challenges associated with Hirschsprung's disease in neonates who initially pass meconium. Timely recognition and surgical intervention achieved a favorable outcome.

摘要

先天性巨结肠症是一种以肠神经节细胞缺失为特征的先天性疾病。在本文中,我们报告了一例8日龄男婴,有便秘和进行性腹胀病史。新生儿病房已排出胎粪。4日龄后未排便,最后一次排便需要直肠刺激。我们强调了在最初排出胎粪的新生儿中诊断先天性巨结肠症所面临的挑战。及时识别和手术干预取得了良好的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/12317170/ea4e073ee030/10.1177_2050313X251360184-fig1.jpg

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