• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

直肠闭锁与先天性甲状腺功能减退症:一种关联还是巧合?

Rectal Atresia and Congenital Hypothyroidism: An Association or Coincidence?

作者信息

Mehmetoğlu Feride

机构信息

Department of Pediatric Surgery, Dortcelik Children's Hospital, Bursa, Turkey.

出版信息

European J Pediatr Surg Rep. 2018 Jan;6(1):e7-e10. doi: 10.1055/s-0037-1612610. Epub 2018 Jan 10.

DOI:10.1055/s-0037-1612610
PMID:29326865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5762197/
Abstract

Rectal atresia is a rare anorectal malformation, and its association with other anomalies is even more rare. This study presents a unique case of co-twin in which the surviving newborn male underwent surgery due to rectal atresia. Newborn screening tests identified congenital hypothyroidism. The surgical treatment consisted of three stages and thyroid hormones were replaced.

摘要

直肠闭锁是一种罕见的肛肠畸形,其与其他异常情况并存则更为罕见。本研究报告了一例独特的联体双胎病例,其中存活的男婴因直肠闭锁接受了手术治疗。新生儿筛查发现先天性甲状腺功能减退。手术治疗分三个阶段进行,并给予甲状腺激素替代治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/7e35e1293084/10-1055-s-0037-1612610-i170353cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/2409c96b8a77/10-1055-s-0037-1612610-i170353cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/7e35e1293084/10-1055-s-0037-1612610-i170353cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/2409c96b8a77/10-1055-s-0037-1612610-i170353cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae2/5762197/7e35e1293084/10-1055-s-0037-1612610-i170353cr-2.jpg

相似文献

1
Rectal Atresia and Congenital Hypothyroidism: An Association or Coincidence?直肠闭锁与先天性甲状腺功能减退症:一种关联还是巧合?
European J Pediatr Surg Rep. 2018 Jan;6(1):e7-e10. doi: 10.1055/s-0037-1612610. Epub 2018 Jan 10.
2
Rectal atresia, choanal atresia and congenital heart disease: a rare association.直肠闭锁、后鼻孔闭锁与先天性心脏病:一种罕见的关联。
Technol Health Care. 2004;12(4):343-5.
3
Rectal Atresia Treated Via a Transanal and Posterior Sagittal Approach: A Report of Two Cases.经肛门及后矢状入路治疗直肠闭锁:两例报告
Cureus. 2023 May 8;15(5):e38694. doi: 10.7759/cureus.38694. eCollection 2023 May.
4
Colonic atresia and anorectal malformation in a Haitian patient: a case study of rare diseases.一名海地患者的结肠闭锁和肛门直肠畸形:罕见疾病的病例研究
Springerplus. 2014 Apr 26;3:203. doi: 10.1186/2193-1801-3-203. eCollection 2014.
5
Congenital rectovestibular fistula associated with rectal atresia: A rare occurrence.先天性直肠前庭瘘合并直肠闭锁:一种罕见的情况。
J Indian Assoc Pediatr Surg. 2013 Jan;18(1):31-2. doi: 10.4103/0971-9261.107015.
6
Rectal atresia and anal stenosis: the difference in the operative technique for these two distinct congenital anorectal malformations.直肠闭锁与肛门狭窄:这两种不同先天性肛肠畸形手术技术的差异。
Tech Coloproctol. 2016 Apr;20(4):249-54. doi: 10.1007/s10151-016-1435-5. Epub 2016 Feb 22.
7
[Rectal mucosa stripping and pull-through from rectal muscle sheath of blind pouch in the treatment of congenital high anal atresia in the newborn].直肠黏膜剥脱并经直肠肌鞘拖出盲袋治疗新生儿先天性高位肛门闭锁
Zhonghua Wei Chang Wai Ke Za Zhi. 2014 Jan;17(1):81-4.
8
An exceptional type of anorectal malformation: anorectal atresia with posterior fistula in a newborn male.一种特殊类型的肛肠畸形:一名男新生儿的肛门直肠闭锁伴后位瘘。
J Pediatr Surg. 2006 Feb;41(2):e7-9. doi: 10.1016/j.jpedsurg.2005.11.049.
9
Rectal atresia.直肠闭锁
J Paediatr Child Health. 2005 Dec;41(12):691-3. doi: 10.1111/j.1440-1754.2005.00763.x.
10
Rare case report of anorectal malformation and intestinal atresia.肛门直肠畸形与肠道闭锁的罕见病例报告。
Int J Surg Case Rep. 2021 May;82:105945. doi: 10.1016/j.ijscr.2021.105945. Epub 2021 Apr 30.

引用本文的文献

1
Outcomes after Surgical Treatment for Rectal Atresia in Children: Is There a Preferred Approach? A Systematic Review.儿童直肠闭锁手术治疗的结果:是否存在首选方法?系统评价。
Eur J Pediatr Surg. 2023 Oct;33(5):345-353. doi: 10.1055/s-0042-1758152. Epub 2022 Dec 14.
2
Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report.先天性直肠狭窄合并唐氏综合征和甲状腺功能减退症的延迟表现:病例报告
Clin Case Rep. 2021 Nov 16;9(11):e05083. doi: 10.1002/ccr3.5083. eCollection 2021 Nov.

本文引用的文献

1
Varied facets of rectal atresia and rectal stenosis.直肠闭锁和直肠狭窄的不同方面。
Pediatr Surg Int. 2017 Aug;33(8):829-836. doi: 10.1007/s00383-017-4106-3. Epub 2017 Jun 10.
2
Pediatric Hypothyroidism: Diagnosis and Treatment.小儿甲状腺功能减退症:诊断与治疗
Paediatr Drugs. 2017 Aug;19(4):291-301. doi: 10.1007/s40272-017-0238-0.
3
Congenital Pouch Colon with Rectal Atresia Revisited.先天性袋状结肠合并直肠闭锁再探讨
J Indian Assoc Pediatr Surg. 2017 Apr-Jun;22(2):119-121. doi: 10.4103/0971-9261.202676.
4
Rectal atresia and anal stenosis: the difference in the operative technique for these two distinct congenital anorectal malformations.直肠闭锁与肛门狭窄:这两种不同先天性肛肠畸形手术技术的差异。
Tech Coloproctol. 2016 Apr;20(4):249-54. doi: 10.1007/s10151-016-1435-5. Epub 2016 Feb 22.
5
Magnamosis: a novel technique for the management of rectal atresia.Magnamosis:一种治疗直肠闭锁的新技术。
BMJ Case Rep. 2014 Aug 5;2014:bcr2013201330. doi: 10.1136/bcr-2013-201330.
6
Rectal atresia: pathogenesis and operative treatment.
Pediatr Surg Int. 1996 Oct;11(8):559-61. doi: 10.1007/BF00626066. Epub 2013 Sep 21.
7
Congenital rectovestibular fistula associated with rectal atresia: A rare occurrence.先天性直肠前庭瘘合并直肠闭锁:一种罕见的情况。
J Indian Assoc Pediatr Surg. 2013 Jan;18(1):31-2. doi: 10.4103/0971-9261.107015.
8
Rectal atresia and stenosis: unique anorectal malformations.直肠闭锁和狭窄:独特的肛门直肠畸形。
J Pediatr Surg. 2012 Jun;47(6):1280-4. doi: 10.1016/j.jpedsurg.2012.03.036.
9
Rectal atresia-operative management with endoscopy and transanal approach: a case report.直肠闭锁的内镜及经肛门手术治疗:一例病例报告
Minim Invasive Surg. 2011;2011:792402. doi: 10.1155/2011/792402. Epub 2011 Apr 21.
10
Comparative outcomes in intestinal atresia: a clinical outcome and pathophysiology analysis.肠闭锁的比较结果:临床结局与病理生理学分析
Pediatr Surg Int. 2011 Apr;27(4):437-42. doi: 10.1007/s00383-010-2729-8. Epub 2010 Sep 4.