A unique case of a newborn with a hemangioma on the omphalocele sac.

IF 0.8 4区 医学 Q4 PEDIATRICS Turkish Journal of Pediatrics Pub Date : 2022-01-01 DOI:10.24953/turkjped.2021.5045
Elif Emel Erten, Can İhsan Öztorun, Süleyman Arif Bostancı, Tuğba Örnek Demir, Medine Ezgi Öcal, Ahmet Ertürk, Sabri Demir, Doğuş Güney, Müjdem Nur Azılı, Emrah Şenel
{"title":"A unique case of a newborn with a hemangioma on the omphalocele sac.","authors":"Elif Emel Erten,&nbsp;Can İhsan Öztorun,&nbsp;Süleyman Arif Bostancı,&nbsp;Tuğba Örnek Demir,&nbsp;Medine Ezgi Öcal,&nbsp;Ahmet Ertürk,&nbsp;Sabri Demir,&nbsp;Doğuş Güney,&nbsp;Müjdem Nur Azılı,&nbsp;Emrah Şenel","doi":"10.24953/turkjped.2021.5045","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Mass lesions of the umbilical cord are rare anomalies. There have been rare reports of hemangiomas of the umbilical cord, but the co-occurrence of omphalocele and hemangioma of the umbilical cord has not been previously reported. Nonetheless, the condition is clinically significant as it may cause the disturbance of intrauterine fetal circulation, retardation of fetal growth and development, non-immune hydrops fetalis, morbidity and mortality.</p><p><strong>Case: </strong>Here we aim to report a case that was prenatally diagnosed with an omphalocele and that presented after birth with a hemangioma on the omphalocele sac.</p><p><strong>Conclusions: </strong>When dealing with umbilical mass lesions in the prenatal and postnatal periods, a hemangioma on the omphalocele sac should be considered in the differential diagnosis of patients when an omphalocele is suspected.</p>","PeriodicalId":49409,"journal":{"name":"Turkish Journal of Pediatrics","volume":"64 5","pages":"935-939"},"PeriodicalIF":0.8000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Pediatrics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.24953/turkjped.2021.5045","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Mass lesions of the umbilical cord are rare anomalies. There have been rare reports of hemangiomas of the umbilical cord, but the co-occurrence of omphalocele and hemangioma of the umbilical cord has not been previously reported. Nonetheless, the condition is clinically significant as it may cause the disturbance of intrauterine fetal circulation, retardation of fetal growth and development, non-immune hydrops fetalis, morbidity and mortality.

Case: Here we aim to report a case that was prenatally diagnosed with an omphalocele and that presented after birth with a hemangioma on the omphalocele sac.

Conclusions: When dealing with umbilical mass lesions in the prenatal and postnatal periods, a hemangioma on the omphalocele sac should be considered in the differential diagnosis of patients when an omphalocele is suspected.

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
新生儿脐膨出囊血管瘤的独特病例。
背景:脐带肿块病变是罕见的异常。脐带血管瘤的报道很少,但脐膨出和脐带血管瘤的同时发生尚未见报道。然而,这种情况在临床上具有重要意义,因为它可能导致宫内胎儿循环障碍,胎儿生长发育迟缓,胎儿非免疫性水肿,发病率和死亡率。病例:在这里,我们的目的是报告一个病例,产前诊断为脐膨出,出生后出现脐膨出囊上的血管瘤。结论:产前产后处理脐肿块病变时,若怀疑脐膨出,应考虑脐囊血管瘤的鉴别诊断。
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 去求助
来源期刊
CiteScore
1.40
自引率
0.00%
发文量
122
审稿时长
6-12 weeks
期刊介绍: The Turkish Journal of Pediatrics is a multidisciplinary, peer reviewed, open access journal that seeks to publish research to advance the field of Pediatrics. The Journal publishes original articles, case reports, review of the literature, short communications, clinicopathological exercises and letter to the editor in the field of pediatrics. Articles published in this journal are evaluated in an independent and unbiased, double blinded peer-reviewed fashion by an advisory committee.
期刊最新文献
Evaluation of thymopoiesis in healthy Turkish children aged 0-6 years. Chronic inflammatory demyelinating polyradiculoneuropathy associated with Sjögren`s syndrome in a child. Celiac disease and catatonia: more than a coincidence? Risk factors for coronary arterial involvement in Turkish children with Kawasaki disease: a multicenter retrospective study. Self-inflicted intravesical insertion of 83 magnetic balls in a 10-year-old boy: a case report and literature review.
×
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