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Metaphyseal chondroblastoma in a pediatric patient
Chondroblastoma is a rare, benign neoplasm usually located in the epiphyses and apophyses of the long bones in the immature skeleton. Radiologically, these tumors have a classic appearance of a lytic lesion with chondroid matrix surrounded by a thin sclerotic rim. Here, we describe the case of a 5-y...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842802/ https://www.ncbi.nlm.nih.gov/pubmed/36660567 http://dx.doi.org/10.1016/j.radcr.2022.12.065 |
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author | Chiesa, Mauricio Paradeda Thompson, Breanna M. Maciel, Natalia Diaz, Dilia Stoppiello, Pablo Gaiero, Leticia Bianchi, Gottardo Casales, Nicolas Silveri, Claudio Belzarena, Ana C. |
author_facet | Chiesa, Mauricio Paradeda Thompson, Breanna M. Maciel, Natalia Diaz, Dilia Stoppiello, Pablo Gaiero, Leticia Bianchi, Gottardo Casales, Nicolas Silveri, Claudio Belzarena, Ana C. |
author_sort | Chiesa, Mauricio Paradeda |
collection | PubMed |
description | Chondroblastoma is a rare, benign neoplasm usually located in the epiphyses and apophyses of the long bones in the immature skeleton. Radiologically, these tumors have a classic appearance of a lytic lesion with chondroid matrix surrounded by a thin sclerotic rim. Here, we describe the case of a 5-year-old male who presented with a chondroblastoma unusually located exclusively in the metaphyseal region, which led to an elusive diagnosis. The presence of tumors outlying the traditional location or epidemiological spectrum, along with the potential for histopathological misdiagnosis, can pose a diagnostic and therapeutic challenge for the treating team. |
format | Online Article Text |
id | pubmed-9842802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98428022023-01-18 Metaphyseal chondroblastoma in a pediatric patient Chiesa, Mauricio Paradeda Thompson, Breanna M. Maciel, Natalia Diaz, Dilia Stoppiello, Pablo Gaiero, Leticia Bianchi, Gottardo Casales, Nicolas Silveri, Claudio Belzarena, Ana C. Radiol Case Rep Case Report Chondroblastoma is a rare, benign neoplasm usually located in the epiphyses and apophyses of the long bones in the immature skeleton. Radiologically, these tumors have a classic appearance of a lytic lesion with chondroid matrix surrounded by a thin sclerotic rim. Here, we describe the case of a 5-year-old male who presented with a chondroblastoma unusually located exclusively in the metaphyseal region, which led to an elusive diagnosis. The presence of tumors outlying the traditional location or epidemiological spectrum, along with the potential for histopathological misdiagnosis, can pose a diagnostic and therapeutic challenge for the treating team. Elsevier 2023-01-12 /pmc/articles/PMC9842802/ /pubmed/36660567 http://dx.doi.org/10.1016/j.radcr.2022.12.065 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Chiesa, Mauricio Paradeda Thompson, Breanna M. Maciel, Natalia Diaz, Dilia Stoppiello, Pablo Gaiero, Leticia Bianchi, Gottardo Casales, Nicolas Silveri, Claudio Belzarena, Ana C. Metaphyseal chondroblastoma in a pediatric patient |
title | Metaphyseal chondroblastoma in a pediatric patient |
title_full | Metaphyseal chondroblastoma in a pediatric patient |
title_fullStr | Metaphyseal chondroblastoma in a pediatric patient |
title_full_unstemmed | Metaphyseal chondroblastoma in a pediatric patient |
title_short | Metaphyseal chondroblastoma in a pediatric patient |
title_sort | metaphyseal chondroblastoma in a pediatric patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842802/ https://www.ncbi.nlm.nih.gov/pubmed/36660567 http://dx.doi.org/10.1016/j.radcr.2022.12.065 |
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