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Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature

Mesenchymal hamartoma of the chest wall is a well-recognized but extremely rare entity. This entity is believed to be benign with no propensity for invasion or metastasis. Although the lesion manifests with alarming aggressive clinical, radiological, and histological features, it is considered benig...

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Autores principales: Alfaraidi, Mona, Alaradati, Hossam, Mamoun, Irfan, Mohammed, Shamayel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576409/
https://www.ncbi.nlm.nih.gov/pubmed/28900550
http://dx.doi.org/10.1155/2017/2876342
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author Alfaraidi, Mona
Alaradati, Hossam
Mamoun, Irfan
Mohammed, Shamayel
author_facet Alfaraidi, Mona
Alaradati, Hossam
Mamoun, Irfan
Mohammed, Shamayel
author_sort Alfaraidi, Mona
collection PubMed
description Mesenchymal hamartoma of the chest wall is a well-recognized but extremely rare entity. This entity is believed to be benign with no propensity for invasion or metastasis. Although the lesion manifests with alarming aggressive clinical, radiological, and histological features, it is considered benign and carries an excellent outcome. Therefore it is important to recognize this benign entity to avoid the possible misdiagnosis of malignancy and the unnecessary use of chemotherapy. We present a case of bilateral multifocal mesenchymal hamartomas of the chest wall in a male infant and a literature review of this entity. Our aim is to improve the awareness of this condition and highlight its benign behavior and satisfactory outcome following complete surgical resection.
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spelling pubmed-55764092017-09-12 Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature Alfaraidi, Mona Alaradati, Hossam Mamoun, Irfan Mohammed, Shamayel Case Rep Pathol Case Report Mesenchymal hamartoma of the chest wall is a well-recognized but extremely rare entity. This entity is believed to be benign with no propensity for invasion or metastasis. Although the lesion manifests with alarming aggressive clinical, radiological, and histological features, it is considered benign and carries an excellent outcome. Therefore it is important to recognize this benign entity to avoid the possible misdiagnosis of malignancy and the unnecessary use of chemotherapy. We present a case of bilateral multifocal mesenchymal hamartomas of the chest wall in a male infant and a literature review of this entity. Our aim is to improve the awareness of this condition and highlight its benign behavior and satisfactory outcome following complete surgical resection. Hindawi 2017 2017-08-16 /pmc/articles/PMC5576409/ /pubmed/28900550 http://dx.doi.org/10.1155/2017/2876342 Text en Copyright © 2017 Mona Alfaraidi et al. https://creativecommons.org/licenses/by/4.0/ 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
Alfaraidi, Mona
Alaradati, Hossam
Mamoun, Irfan
Mohammed, Shamayel
Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title_full Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title_fullStr Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title_full_unstemmed Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title_short Bilateral Mesenchymal Hamartoma of the Chest Wall in a 3-Month-Old Boy: A Case Report and Review of the Literature
title_sort bilateral mesenchymal hamartoma of the chest wall in a 3-month-old boy: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576409/
https://www.ncbi.nlm.nih.gov/pubmed/28900550
http://dx.doi.org/10.1155/2017/2876342
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