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卵黄管未闭

Patent vitellointestinal duct.

作者信息

Agrawal Sanwar, Memon Ameen

机构信息

Department of Pediatrics, Ekta Institute of Child Health, Raipur, India.

出版信息

BMJ Case Rep. 2010 Oct 6;2010:bcr1220092594. doi: 10.1136/bcr.12.2009.2594.

DOI:10.1136/bcr.12.2009.2594
PMID:22778111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3029414/
Abstract

During the 3rd week of intrauterine life there is a communication between the intraembryonic gut and the yolk sac. As the development proceeds this communication narrows into a tube known as the vitellointestinal duct (VID). With the establishment of placental nutrition this duct usually becomes obliterated by the end of the 7th week of intrauterine life. In about 2% of humans this duct persists and gives rise to a group of anomalies of which Meckel's diverticulum is the commonest and complete patency of the duct is the rarest.1 We report a case of a 4-month-old infant who presented with umbilical polyp, discharge from the umbilicus, significant dehydration and failure to thrive because of complete patency of the VID.

摘要

在子宫内生活的第3周,胚胎内肠道与卵黄囊之间存在连通。随着发育的进行,这种连通逐渐变窄形成一条称为卵黄肠管(VID)的管道。随着胎盘营养的建立,这条管道通常在子宫内生活第7周结束时闭塞。在大约2%的人类中,这条管道会持续存在,并引发一系列异常情况,其中梅克尔憩室最为常见,而管道完全通畅则最为罕见。1我们报告一例4个月大婴儿的病例,该婴儿因卵黄肠管完全通畅而出现脐息肉、脐部排出物、严重脱水及发育不良。

相似文献

1
Patent vitellointestinal duct.卵黄管未闭
BMJ Case Rep. 2010 Oct 6;2010:bcr1220092594. doi: 10.1136/bcr.12.2009.2594.
2
Coexistence of multiple omphalomesenteric duct anomalies.多种脐肠系膜管异常并存。
J Coll Physicians Surg Pak. 2012 Aug;22(8):524-6.
3
Neonatal prolapsed patent vitellointestinal duct.新生儿卵黄管脱垂
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A rare case report of patent vitellointestinal duct presenting as a periumbilical pain in an adult.一例罕见的成人卵黄管未闭表现为脐周疼痛的病例报告。
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Vitello-intestinal duct fistula--a rare presentation of a patent vitello-intestinal duct: a case report.卵黄管瘘——卵黄管未闭的一种罕见表现:病例报告
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Patent vitellointestinal duct with ileal prolapse in a newborn: A case report and literature review.新生儿先天性脐肠系膜管突出并回肠脱出 1 例报告并文献复习
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Prolapse of inverted ileal loops through a patent vitellointestinal duct.倒置的回肠袢经卵黄肠管未闭处脱垂。
BMJ Case Rep. 2015 Oct 22;2015:bcr2015211563. doi: 10.1136/bcr-2015-211563.
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Surgical treatment of patent omphalomesenteric duct presenting as faecal umbilical discharge.以脐部粪便样分泌物为表现的卵黄管未闭的外科治疗
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A newer surgical approach for patent vitello-intestinal duct anomalies.一种针对卵黄管未闭异常的新型手术方法。
Surg Gynecol Obstet. 1991 Jul;173(1):69-70.
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Omphalomesenteric duct malformations.脐肠系膜管畸形。
Semin Pediatr Surg. 1996 May;5(2):116-23.

引用本文的文献

1
Persistent omphalomesenteric duct in an infant with trisomy 21.21 三体婴儿持续性脐肠系膜管。
BMJ Case Rep. 2024 May 8;17(5):e259671. doi: 10.1136/bcr-2024-259671.
2
A rare case report of patent vitellointestinal duct presenting as a periumbilical pain in an adult.一例罕见的成人卵黄管未闭表现为脐周疼痛的病例报告。
Radiol Case Rep. 2024 Jan 20;19(4):1476-1479. doi: 10.1016/j.radcr.2024.01.003. eCollection 2024 Apr.
3
Patent vitellointestinal duct with ileal prolapse in a newborn: A case report and literature review.新生儿先天性脐肠系膜管突出并回肠脱出 1 例报告并文献复习
Medicine (Baltimore). 2024 Jan 19;103(3):e36919. doi: 10.1097/MD.0000000000036919.
4
Omphalomesenteric duct resection using an intraumbilical round incision or a transumbilical vertical incision: report of two cases.采用脐部环形切口或经脐垂直切口行卵黄管切除术:2例报告
J Surg Case Rep. 2020 Oct 28;2020(10):rjaa428. doi: 10.1093/jscr/rjaa428. eCollection 2020 Oct.
5
Umbilical cord anomalies: antenatal ultrasound findings and postnatal correlation.脐带异常:产前超声检查结果与产后相关性
BMJ Case Rep. 2018 Oct 25;2018:bcr-2018-226651. doi: 10.1136/bcr-2018-226651.
6
Prolapse of inverted ileal loops through a patent vitellointestinal duct.倒置的回肠袢经卵黄肠管未闭处脱垂。
BMJ Case Rep. 2015 Oct 22;2015:bcr2015211563. doi: 10.1136/bcr-2015-211563.
7
Patent vitellointestinal duct as paraumblical abcess: A rare presentation.卵黄管未闭并发脐旁脓肿:一种罕见的表现。
Int J Surg Case Rep. 2015;15:30-1. doi: 10.1016/j.ijscr.2015.07.039. Epub 2015 Aug 14.
8
Neonatal prolapsed patent vitellointestinal duct.新生儿卵黄管脱垂
BMJ Case Rep. 2013 Jul 10;2013:bcr2013010221. doi: 10.1136/bcr-2013-010221.

本文引用的文献

1
Patent vitello-intestinal duct.卵黄管未闭
Indian J Pediatr. 1979 Jun;46(377):215-8. doi: 10.1007/BF02898231.