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胸廓裂的产前诊断及文献综述

Prenatal Diagnosis of Thoracoschisis and Review of Literature.

作者信息

Hanafi Hasaruddin R, Zakaria Zahar A

机构信息

Paediatric Department, Hospital Kemaman, Terengganu, Malaysia.

Obstetrics & Gynaecology Department, Hospital Kemaman, Terengganu, Malaysia.

出版信息

Case Rep Obstet Gynecol. 2017;2017:9821213. doi: 10.1155/2017/9821213. Epub 2017 Nov 16.

DOI:10.1155/2017/9821213
PMID:29348951
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5733959/
Abstract

Thoracoschisis is a rare congenital malformation characterized by herniation of the abdominal content through a defect in the thorax. There are previously 12 reported cases, most discussing the postnatal findings and management. Here we describe a case of left thoracoschisis with associated upper limb abnormality which was diagnosed antenatally with the aid of 3D ultrasound.

摘要

胸廓裂是一种罕见的先天性畸形,其特征为腹腔内容物通过胸部的缺损疝出。此前有12例报告病例,大多讨论的是产后的发现和处理。在此,我们描述一例伴有上肢异常的左侧胸廓裂病例,该病例在三维超声的辅助下于产前得到诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/3c9cfbb95a98/CRIOG2017-9821213.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/940e2b11ccf7/CRIOG2017-9821213.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/f440a9ef8d76/CRIOG2017-9821213.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/97cc01e5276e/CRIOG2017-9821213.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/3c9cfbb95a98/CRIOG2017-9821213.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/940e2b11ccf7/CRIOG2017-9821213.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/f440a9ef8d76/CRIOG2017-9821213.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/97cc01e5276e/CRIOG2017-9821213.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb34/5733959/3c9cfbb95a98/CRIOG2017-9821213.004.jpg

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本文引用的文献

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2
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3
Isolated Thoracoschisis: Case Report and Review of Literature.孤立性胸裂:病例报告及文献综述
European J Pediatr Surg Rep. 2015 Jun;3(1):40-2. doi: 10.1055/s-0034-1396013. Epub 2014 Dec 3.
4
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J Indian Assoc Pediatr Surg. 2012 Apr;17(2):78-9. doi: 10.4103/0971-9261.93972.
5
First-trimester diagnosis of body stalk anomaly using 2- and 3-dimensional sonography.早孕期应用二维和三维超声诊断体蒂异常。
J Ultrasound Med. 2011 Dec;30(12):1739-43. doi: 10.7863/jum.2011.30.12.1739.
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The first male with thoracoschisis: case report and review of the literature.首例胸腰裂患者:病例报告及文献复习。
J Pediatr Surg. 2011 Nov;46(11):2181-3. doi: 10.1016/j.jpedsurg.2011.08.016.
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A new syndrome with prenatally diagnosed thoracoschisis, hiatal hernia and extremities' agenesis: case report.一种产前诊断为胸裂、食管裂孔疝和肢体发育不全的新综合征:病例报告。
Genet Couns. 2006;17(2):161-5.
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Am J Obstet Gynecol. 1965 Jan 1;91:65-75. doi: 10.1016/0002-9378(65)90588-0.
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Thoracoschisis associated with diaphragmatic hernia in a 31-week-old stillbirth.一名31周死产儿的胸廓裂合并膈疝。
Turk J Pediatr. 2001 Jul-Sep;43(3):269-71.
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Vascular pathogenesis of limb defects. I. Radial artery anatomy in radial aplasia.肢体缺陷的血管发病机制。I. 桡骨发育不全时的桡动脉解剖结构。
J Pediatr. 1982 Nov;101(5):832-8. doi: 10.1016/s0022-3476(82)80342-9.