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Lack of BRAF mutations in hyalinizing trabecular neoplasm
The hyalinizing trabecular neoplasm (HTN) of the thyroid is an unusual and controversial lesion. Some consider it a peculiar type of papillary thyroid carcinoma (PTC) because of its nuclear features and presence of psammoma bodies. Others consider it an adenoma. Molecular studies have found RET/PTC...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1544348/ https://www.ncbi.nlm.nih.gov/pubmed/16867191 http://dx.doi.org/10.1186/1742-6413-3-17 |
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author | Baloch, Zubair W Puttaswamy, Kanchan Brose, Marcia LiVolsi, Virginia A |
author_facet | Baloch, Zubair W Puttaswamy, Kanchan Brose, Marcia LiVolsi, Virginia A |
author_sort | Baloch, Zubair W |
collection | PubMed |
description | The hyalinizing trabecular neoplasm (HTN) of the thyroid is an unusual and controversial lesion. Some consider it a peculiar type of papillary thyroid carcinoma (PTC) because of its nuclear features and presence of psammoma bodies. Others consider it an adenoma. Molecular studies have found RET/PTC translocations in some examples, supporting HTN as a PTC; however mutations in BRAF (another marker for PTC) have not been found. We report two cases of classic HTN and a case of trabecular PTC and show BRAF mutations in the latter and not in HTN. Trabecular growth pattern is insufficient for a diagnosis of HTN and lesions with such a pattern and nuclear features of PTC are cancers. Morphologically classic HTN are not associated with metastatic potential and should be considered adenomas. |
format | Text |
id | pubmed-1544348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15443482006-08-16 Lack of BRAF mutations in hyalinizing trabecular neoplasm Baloch, Zubair W Puttaswamy, Kanchan Brose, Marcia LiVolsi, Virginia A Cytojournal Case Report The hyalinizing trabecular neoplasm (HTN) of the thyroid is an unusual and controversial lesion. Some consider it a peculiar type of papillary thyroid carcinoma (PTC) because of its nuclear features and presence of psammoma bodies. Others consider it an adenoma. Molecular studies have found RET/PTC translocations in some examples, supporting HTN as a PTC; however mutations in BRAF (another marker for PTC) have not been found. We report two cases of classic HTN and a case of trabecular PTC and show BRAF mutations in the latter and not in HTN. Trabecular growth pattern is insufficient for a diagnosis of HTN and lesions with such a pattern and nuclear features of PTC are cancers. Morphologically classic HTN are not associated with metastatic potential and should be considered adenomas. BioMed Central 2006-07-25 /pmc/articles/PMC1544348/ /pubmed/16867191 http://dx.doi.org/10.1186/1742-6413-3-17 Text en Copyright © 2006 Baloch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Baloch, Zubair W Puttaswamy, Kanchan Brose, Marcia LiVolsi, Virginia A Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title | Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title_full | Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title_fullStr | Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title_full_unstemmed | Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title_short | Lack of BRAF mutations in hyalinizing trabecular neoplasm |
title_sort | lack of braf mutations in hyalinizing trabecular neoplasm |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1544348/ https://www.ncbi.nlm.nih.gov/pubmed/16867191 http://dx.doi.org/10.1186/1742-6413-3-17 |
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