尼日利亚乔斯市新生儿期出现的先天性巨结肠病

L. Chirdan, A. Uba
{"title":"尼日利亚乔斯市新生儿期出现的先天性巨结肠病","authors":"L. Chirdan, A. Uba","doi":"10.4314/NJSR.V8I1.54825","DOIUrl":null,"url":null,"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.","PeriodicalId":19188,"journal":{"name":"Nigerian Journal of Surgical Research","volume":"31 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2010-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":"{\"title\":\"Hirschsprung’s disease presenting in the neonatal period in Jos,Nigeria\",\"authors\":\"L. Chirdan, A. Uba\",\"doi\":\"10.4314/NJSR.V8I1.54825\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":19188,\"journal\":{\"name\":\"Nigerian Journal of Surgical Research\",\"volume\":\"31 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nigerian Journal of Surgical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4314/NJSR.V8I1.54825\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nigerian Journal of Surgical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4314/NJSR.V8I1.54825","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

摘要

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。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Hirschsprung’s disease presenting in the neonatal period in Jos,Nigeria
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Utero-cutaneous fistula following cesarean section Pattern of traumatic spinal cord injury in Makurdi, Nigeria Prevalence and attitude of self-ear cleaning with cotton bud among doctors at aminu Kano teaching hospital, Northwestern Nigeria Caudal regression syndrome with a solitary kidney: A case report and review of the literature Simultaneous bilateral femoral neck fractures following electroconvulsive therapy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1