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间叶性错构瘤：通过影像学进行产前和产后诊断

Mesenchymal hamartoma: prenatal and postnatal diagnosis by imaging.

作者信息

Martínez-Varea Alicia, Vila-Vives Jose María, Hidalgo-Mora Juan José, Abad-Carrascosa Antonio, Llorens-Salvador Roberto, Perales-Marín Alfredo

机构信息

Department of Obstetrics and Gynecology, La Fe University Hospital, 46026 Valencia, Spain.

出版信息

Case Rep Obstet Gynecol. 2012;2012:954241. doi: 10.1155/2012/954241. Epub 2012 Dec 5.

DOI:10.1155/2012/954241
PMID:23259097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3521408/
Abstract

We present a case of a twin pregnancy in which one fetus developed a rapidly growing unilateral intrathoracic tumor. While a cystic adenomatoid malformation was suspected in the ultrasound scan, the magnetic resonance scan suggested a pulmonary blastoma or a bronchioalveolar carcinoma. Postnatal chest radiography and contrast-enhanced computed tomography of the affected newborn were performed, and it was ruled out the possibility of malignant origin. Finally, the anatomopathologic exam revealed the presence of a mesenchymal hamartoma in the chest wall. Nevertheless, parents refused any treatment for the newborn.

摘要

我们报告一例双胎妊娠病例，其中一个胎儿发生了一个快速生长的单侧胸腔内肿瘤。超声扫描怀疑为囊性腺瘤样畸形，而磁共振扫描提示为肺母细胞瘤或细支气管肺泡癌。对受影响的新生儿进行了产后胸部X线摄影和增强计算机断层扫描，排除了恶性起源的可能性。最后，解剖病理学检查显示胸壁存在间叶性错构瘤。然而，父母拒绝为新生儿进行任何治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/316e0359353f/CRIM.OBGYN2012-954241.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/563d99facfab/CRIM.OBGYN2012-954241.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/8c9897cde0a5/CRIM.OBGYN2012-954241.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/316e0359353f/CRIM.OBGYN2012-954241.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/563d99facfab/CRIM.OBGYN2012-954241.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/8c9897cde0a5/CRIM.OBGYN2012-954241.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dcc/3521408/316e0359353f/CRIM.OBGYN2012-954241.003.jpg

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本文引用的文献

1
Prenatal diagnosis of congenital lung malformations.先天性肺畸形的产前诊断。
Pediatr Radiol. 2012 Mar;42(3):273-83. doi: 10.1007/s00247-011-2303-0. Epub 2012 Jan 20.
2
Perinatal evolution of mesenchymal hamartoma of the chest wall.胸腔壁间叶性错构瘤的围生期演变。
J Pediatr Surg. 2010 Dec;45(12):e37-40. doi: 10.1016/j.jpedsurg.2010.08.057.
3
Mesenchymal hamartoma: prenatal diagnosis by MRI.间叶性错构瘤：MRI 产前诊断。
Pediatr Radiol. 2011 Jun;41(6):781-4. doi: 10.1007/s00247-010-1898-x. Epub 2010 Dec 1.
4
Antenatal diagnosis of congenital thoracic malformations: early surgery, late surgery, or no surgery?先天性胸部畸形的产前诊断：早期手术、晚期手术还是不手术？
Semin Respir Crit Care Med. 2007 Jun;28(3):355-66. doi: 10.1055/s-2007-981656.
5
Respiratory insufficiency in a newborn with mesenchymal hamartoma of the chest wall occupying the thoracic cavity.
J Pediatr Surg. 2005 Apr;40(4):E13-6. doi: 10.1016/j.jpedsurg.2005.01.022.
6
From the archives of the AFIP: a comprehensive review of fetal tumors with pathologic correlation.源自武装部队病理研究所档案：胎儿肿瘤的全面回顾及病理对照
Radiographics. 2005 Jan-Feb;25(1):215-42. doi: 10.1148/rg.251045156.
7
Mesenchymal hamartoma of the chest wall: radiologic manifestations with emphasis on cross-sectional imaging and histopathologic comparison.胸壁间叶性错构瘤：影像学表现，重点是横断面成像及组织病理学比较
Radiology. 2002 Jan;222(1):205-11. doi: 10.1148/radiol.2221010522.
8
Outcome of the prenatally diagnosed congenital cystic adenomatoid lung malformation: a Canadian experience.产前诊断的先天性肺囊性腺瘤样畸形的结局：加拿大的经验
Fetal Diagn Ther. 2001 May-Jun;16(3):178-86. doi: 10.1159/000053905.