Motility malfunction of the gastrointestinal tract by rare diseases--fibrosis of the intestinal wall.

R Daum, W Nützenadel, H Roth, Z Zachariou
{"title":"Motility malfunction of the gastrointestinal tract by rare diseases--fibrosis of the intestinal wall.","authors":"R Daum,&nbsp;W Nützenadel,&nbsp;H Roth,&nbsp;Z Zachariou","doi":"10.1007/978-3-642-74493-8_21","DOIUrl":null,"url":null,"abstract":"<p><p>We report on two children who were admitted with chronic ileus without mechanical obstruction. In the 4-month-old female newborn, high-dose radiation was applied after extirpation of a sympathicoblastoma. Within a few years a metaplasia of the muscle coat of the small intestine developed with a resulting malabsorption syndrome. Although the damaged part of the intestine was resected, the process progressed and the child died. In the second case, a chronic ileus developed at the age of 10 years as a result of fibrosis of the intestinal tract. Repeated laparotomies were performed, and no mechanical obstruction could be found. The most probable diagnosis is a form of scleroderma affecting mainly the alimentary tract without any skin involvement. The patient died in a severe cachexia.</p>","PeriodicalId":76378,"journal":{"name":"Progress in pediatric surgery","volume":"24 ","pages":"193-201"},"PeriodicalIF":0.0000,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in pediatric surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-642-74493-8_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

We report on two children who were admitted with chronic ileus without mechanical obstruction. In the 4-month-old female newborn, high-dose radiation was applied after extirpation of a sympathicoblastoma. Within a few years a metaplasia of the muscle coat of the small intestine developed with a resulting malabsorption syndrome. Although the damaged part of the intestine was resected, the process progressed and the child died. In the second case, a chronic ileus developed at the age of 10 years as a result of fibrosis of the intestinal tract. Repeated laparotomies were performed, and no mechanical obstruction could be found. The most probable diagnosis is a form of scleroderma affecting mainly the alimentary tract without any skin involvement. The patient died in a severe cachexia.

罕见疾病引起的胃肠道运动障碍——肠壁纤维化。
我们报告两名儿童谁是入院慢性肠梗阻没有机械阻塞。在4个月大的女性新生儿中,切除交感母细胞瘤后应用高剂量辐射。在几年内,小肠肌层发生化生,导致吸收不良综合征。虽然受损的肠道部分被切除了,但手术仍在继续,孩子最终死亡。在第二个病例中,慢性肠梗阻在10岁时发展为肠道纤维化的结果。多次开腹手术均未发现机械性梗阻。最可能的诊断是一种硬皮病,主要影响消化道,不累及皮肤。病人死于严重的恶病质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信