Hirschsprung’s disease presenting in the neonatal period in Jos,Nigeria

L. Chirdan, A. Uba
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引用次数: 10

Abstract

Background : While most cases of Hirschsprung’s disease are diagnosed during the neonatal period in developed countries, majority of the cases present outside the neonatal period in developing countries. We reviewed our experience with Hirschsprung’s disease presenting during the neonatal period to document the presentation and management. Patients/Methods : A retrospective analysis of the presentation and management of 31 neonates with Hirschsprung’s disease over a nine year period in a Tertiary pediatric surgical centre in Nigeria was performed. Results : From January 1996 – December 2004, 78 children were managed for Hirschsprung’s disease in our unit. Thirty-one (39.7%) were aged 30 days or below. The median age at presentation was eight days (range 2-30 days). There were 23 boys and 8 girls. The median weight at presentation was 2.8kg (range 2.3 – 4.5kg). Fifteen weighed presented with enterocolitis while in five there was delayed passage of meconium and recurrent constipation. Barium enema was done in 25 and rectal biopsy confirmed diagnosis in 29 babies. In two babies with total colonic aganglionosis (TCA), diagnosis was confirmed by colonic biopsy at laparotomy. Twenty nine had right transverse loop colostomy in the neonatal period; four were under local anesthesia, while the two children with TCA had ileostomy. Four children died before definitive surgery, two with TCA and two with enterocolitis. None had primary pull-through. Two children were lost to follow up after colostomy formation. Twenty two had definitive surgery between the ages of three months and five years. Fifteen had Boley’s endorectal pull-through with a single mortality; while seven had Swenson’s pull-through, one of whom died. Conclusion : Few cases of Hirschsprung’s disease present during the neonatal period in our environment, many presenting with intestinal obstruction. A high index of suspicion is needed for the early diagnosis of Hirschsprung’s disease in environment with limited diagnostic facilities.
尼日利亚乔斯市新生儿期出现的先天性巨结肠病
背景:在发达国家,大多数先天性巨结肠病例是在新生儿期诊断出来的,而在发展中国家,大多数病例出现在新生儿期之外。我们回顾了我们的经验与先天性巨结肠疾病在新生儿时期提出的文件的表现和管理。患者/方法:回顾性分析了尼日利亚一家三级儿科外科中心9年来31例先天性巨结肠新生儿的表现和治疗。结果:1996年1月至2004年12月,本科收治先天性巨结肠患儿78例。年龄在30天或以下的31只(39.7%)。发病时的中位年龄为8天(范围2-30天)。有23个男孩和8个女孩。患者就诊时的中位体重为2.8kg(范围2.3 - 4.5kg)。15名体重正常的患者出现小肠结肠炎,5名出现胎便排便延迟和反复便秘。25例行钡灌肠,29例经直肠活检确诊。在两名患有全结肠神经节病(TCA)的婴儿中,在剖腹手术中通过结肠活检确诊。29例在新生儿期行右横环结肠造口术;4例局部麻醉,2例行回肠造口术。4名儿童在最终手术前死亡,2名患有TCA, 2名患有小肠结肠炎。没有一个是主要的拉通。2例患儿在结肠造口术后未随访。22人在3个月到5岁之间进行了最终手术。15例有Boley式直肠内拉通,一例死亡;而有7人和斯文森一样成功脱险,其中一人死亡。结论:在我们的环境中,先天性巨结肠在新生儿时期很少出现,多数表现为肠梗阻。在诊断设备有限的环境下,对巨结肠的早期诊断需要高度的怀疑指数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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