• 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

肢体-体壁复合体的产前超声诊断：罕见先天性异常病例系列

Prenatal sonographic diagnosis of limb-body wall complex: case series of a rare congenital anomaly.

作者信息

Bhat Arshad, Ilyas Mohd, Dev Ghanshyam

机构信息

Department of Radiodiagnosis and Imaging, SMGS Hospital, Govt. Medical College and Associated Hospitals, Jammu, 180001, India.

Department of Radiodiagnosis and Imaging, Govt. Medical College and Associated Hospitals, Jammu, Lane 22, House No. 38, Tawi Vihar, Sidhra, Jammu, 180001, India.

出版信息

Radiol Case Rep. 2016 Mar 15;11(2):116-20. doi: 10.1016/j.radcr.2016.02.004. eCollection 2016 Jun.

DOI:10.1016/j.radcr.2016.02.004
PMID:27257465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4878923/
Abstract

Three case reports of a rare congenital anomaly "limb-body wall complex" also known as "body stalk syndrome" are presented with prenatal ultrasonographic diagnostic features, immediate after delivery evaluation, and histopathologic analysis.

摘要

本文报告了三例罕见的先天性异常“肢体-体壁复合体”（又称“体蒂综合征”）的病例，介绍了其产前超声诊断特征、产后即刻评估及组织病理学分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/1730803c6d65/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/54338c995cf9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/5eaee6c2617d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/1730803c6d65/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/54338c995cf9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/5eaee6c2617d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbb4/4878923/1730803c6d65/gr3.jpg

相似文献

1
Prenatal sonographic diagnosis of limb-body wall complex: case series of a rare congenital anomaly.肢体-体壁复合体的产前超声诊断：罕见先天性异常病例系列
Radiol Case Rep. 2016 Mar 15;11(2):116-20. doi: 10.1016/j.radcr.2016.02.004. eCollection 2016 Jun.
2
BODY STALK ANOMALY: CLINICAL AND HISTOPATHOLOGIC FINDINGS OF THIS RARE ANOMALY IN A NIGERIAN NEWBORN.体蒂异常：一名尼日利亚新生儿中这种罕见异常的临床和组织病理学发现
Ann Ib Postgrad Med. 2024 Apr 30;22(1):104-107.
3
Prenatal ultrasound diagnosis and management of body stalk anomaly: analysis of nine singleton and two multiple pregnancies.体蒂异常的产前超声诊断与处理：9例单胎妊娠及2例多胎妊娠分析
Ultrasound Obstet Gynecol. 2003 Apr;21(4):322-8. doi: 10.1002/uog.84.
4
Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex) with overlapping features of body stalk anomaly (limb body wall complex).脐膨出、泄殖腔外翻、肛门闭锁和脊柱缺损（OEIS综合征）并伴有体蒂异常（肢体-体壁综合征）的重叠特征。
Indian J Hum Genet. 2014 Apr;20(2):195-8. doi: 10.4103/0971-6866.142906.
5
Body Stalk Anomaly.体蒂异常
Diagnostics (Basel). 2024 Feb 29;14(5):518. doi: 10.3390/diagnostics14050518.
6
Body stalk anomaly: antenatal sonographic diagnosis of this rare entity with review of literature.躯体蒂异常：该罕见实体的产前超声诊断及文献复习
J Ultrason. 2017 Jun;17(69):133-135. doi: 10.15557/JoU.2017.0020. Epub 2017 Jun 30.
7
Limb-body wall complex: in utero sonographic diagnosis of a complicated fetal malformation.肢体-体壁复合体：宫内超声诊断复杂胎儿畸形
AJR Am J Roentgenol. 1986 May;146(5):1019-24. doi: 10.2214/ajr.146.5.1019.
8
Dichorionic twins discordant for body-stalk anomaly: a management challenge.双绒毛膜双胎中一胎出现体蒂异常：管理挑战
BMJ Case Rep. 2018 May 12;2018:bcr-2017-223825. doi: 10.1136/bcr-2017-223825.
9
[Body stalk anomaly--a case report on a rare congenital defect].[躯体蒂异常——一例罕见先天性缺陷病例报告]
Zentralbl Gynakol. 2006 Dec;128(6):369-71. doi: 10.1055/s-2006-933425.
10
Fetal abdominal wall defects.胎儿腹壁缺陷。
Best Pract Res Clin Obstet Gynaecol. 2014 Apr;28(3):391-402. doi: 10.1016/j.bpobgyn.2013.10.003. Epub 2013 Dec 3.

引用本文的文献

1
Characteristic Analysis of Ultrasound Diagnosis of Limb Body Wall Complex in Early Pregnancy.早孕期肢体-体壁复合体超声诊断的特征分析
Prenat Diagn. 2025 Jul;45(8):1004-1012. doi: 10.1002/pd.6808. Epub 2025 May 7.
2
A Rare Case Report of Limb Body Wall Complex.肢体-体壁复合畸形的罕见病例报告
Cureus. 2024 Apr 25;16(4):e59026. doi: 10.7759/cureus.59026. eCollection 2024 Apr.
3
Analysis of characteristic features in ultrasound diagnosis of fetal limb body wall complex during 11-13 weeks.孕11-13周胎儿肢体-体壁复合体超声诊断特征分析

本文引用的文献

1
Limb Body Wall Complex.肢体-体壁复合体
Med J Armed Forces India. 2004 Jan;60(1):77-80. doi: 10.1016/S0377-1237(04)80169-2. Epub 2011 Jul 21.
2
Prenatal diagnosis of body stalk complex: A rare entity and review of literature.体蒂异常复合体的产前诊断：一种罕见病例及文献综述
Indian J Radiol Imaging. 2015 Jan-Mar;25(1):67-70. doi: 10.4103/0971-3026.150162.
3
Limb body wall complex in a still born fetus: a case report.死产胎儿肢体-体壁复合体：一例报告
World J Clin Cases. 2023 Jul 6;11(19):4544-4552. doi: 10.12998/wjcc.v11.i19.4544.
4
Anatomy-based diagnostic criteria for complex body wall anomalies (CBWA).基于解剖学的复杂体壁异常（CBWA）诊断标准。
Mol Genet Genomic Med. 2020 Oct;8(10):e1465. doi: 10.1002/mgg3.1465. Epub 2020 Aug 27.
5
Fetal MRI in the Identification of a Fetal Ventral Wall Defect Spectrum.胎儿磁共振成像在胎儿腹壁缺损谱系识别中的应用
AJP Rep. 2018 Oct;8(4):e264-e276. doi: 10.1055/s-0038-1675353. Epub 2018 Oct 29.
Cases J. 2008 Aug 12;1(1):86. doi: 10.1186/1757-1626-1-86.
4
Prenatal ultrasonographical features of limb body wall complex: a review of etiopathogenesis and a new classification.肢体-体壁复合体的产前超声特征：病因学及新分类的综述
Fetal Pediatr Pathol. 2007 May-Jun;26(3):135-51. doi: 10.1080/15513810701563728.
5
Limb-body wall complex, report of 2 cases with their quintessence in prenatal diagnosis.肢体-体壁综合征，2例报告及其产前诊断要点
J Med Assoc Thai. 2001 Apr;84(4):602-8.
6
Limb body wall complex: I. Pathogenesis.肢体-体壁复合畸形：I. 发病机制。
Am J Med Genet. 1987 Nov;28(3):529-48. doi: 10.1002/ajmg.1320280302.
7
Limb-body wall complex: in utero sonographic diagnosis of a complicated fetal malformation.肢体-体壁复合体：宫内超声诊断复杂胎儿畸形
AJR Am J Roentgenol. 1986 May;146(5):1019-24. doi: 10.2214/ajr.146.5.1019.
8
Limb body wall malformation complex: an embryologic etiology?肢体-体壁复合畸形：一种胚胎学病因？
Hum Pathol. 1989 Nov;20(11):1071-7. doi: 10.1016/0046-8177(89)90225-6.