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Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging

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 che...

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Autores principales: Martínez-Varea, Alicia, Vila-Vives, Jose María, Hidalgo-Mora, Juan José, Abad-Carrascosa, Antonio, Llorens-Salvador, Roberto, Perales-Marín, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521408/
https://www.ncbi.nlm.nih.gov/pubmed/23259097
http://dx.doi.org/10.1155/2012/954241
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author Martínez-Varea, Alicia
Vila-Vives, Jose María
Hidalgo-Mora, Juan José
Abad-Carrascosa, Antonio
Llorens-Salvador, Roberto
Perales-Marín, Alfredo
author_facet Martínez-Varea, Alicia
Vila-Vives, Jose María
Hidalgo-Mora, Juan José
Abad-Carrascosa, Antonio
Llorens-Salvador, Roberto
Perales-Marín, Alfredo
author_sort Martínez-Varea, Alicia
collection PubMed
description 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.
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spelling pubmed-35214082012-12-20 Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging Martínez-Varea, Alicia Vila-Vives, Jose María Hidalgo-Mora, Juan José Abad-Carrascosa, Antonio Llorens-Salvador, Roberto Perales-Marín, Alfredo Case Rep Obstet Gynecol Case Report 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. Hindawi Publishing Corporation 2012 2012-12-05 /pmc/articles/PMC3521408/ /pubmed/23259097 http://dx.doi.org/10.1155/2012/954241 Text en Copyright © 2012 Alicia Martínez-Varea et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Martínez-Varea, Alicia
Vila-Vives, Jose María
Hidalgo-Mora, Juan José
Abad-Carrascosa, Antonio
Llorens-Salvador, Roberto
Perales-Marín, Alfredo
Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title_full Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title_fullStr Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title_full_unstemmed Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title_short Mesenchymal Hamartoma: Prenatal and Postnatal Diagnosis by Imaging
title_sort mesenchymal hamartoma: prenatal and postnatal diagnosis by imaging
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521408/
https://www.ncbi.nlm.nih.gov/pubmed/23259097
http://dx.doi.org/10.1155/2012/954241
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