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Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them
BACKGROUND: Much discussion about benign notochordal cell tissue in vertebrae has centered on the nature of its relationship, if any, to chordoma. Often referred to as benign notochordal cell tumors (BNCTs), these lesions have unique morphological features, however, differentiating between notochord...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212531/ https://www.ncbi.nlm.nih.gov/pubmed/25609192 http://dx.doi.org/10.1186/1470-7330-14-4 |
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author | Kreshak, Jennifer Larousserie, Frédérique Picci, Piero Boriani, Stefano Mirra, Joseph Merlino, Biagio Brunocilla, Eugenio Vanel, Daniel |
author_facet | Kreshak, Jennifer Larousserie, Frédérique Picci, Piero Boriani, Stefano Mirra, Joseph Merlino, Biagio Brunocilla, Eugenio Vanel, Daniel |
author_sort | Kreshak, Jennifer |
collection | PubMed |
description | BACKGROUND: Much discussion about benign notochordal cell tissue in vertebrae has centered on the nature of its relationship, if any, to chordoma. Often referred to as benign notochordal cell tumors (BNCTs), these lesions have unique morphological features, however, differentiating between notochordal cells in discs, BNCT, and chordoma can be difficult. They are described as radiologically distinct from chordoma, with lysis, contrast enhancement, and a soft tissue mass indicating chordoma. METHODS: All chordomas diagnosed at our institution, the Istituto Ortopedico Rizzoli (Bologna, Italy), prior to 2008 were reviewed, yielding 174 cases. Five were limited to bone; one was a recurrent chordoma without original data available. The remaining four were re-evaluated in detail. RESULTS: There were three women and one man, aged 33–57 years (mean, 48 years). Two were BNCTs and two were mixed lesions containing BNCT and chordoma. On computed tomography, all were radiopaque with areas of lysis. One BNCT was heterogeneous on magnetic resonance imaging, enhancing after contrast. Microscopically, one BNCT had a well-defined cystic area with a sclerotic border. The other had a minute atypical area; it recurred as chordoma. The mixed lesions had areas of definitive BNCT, definitive chordoma, and atypical areas that did not meet the criteria for either. The atypical areas in all three cases ‘blended’ with areas of chordoma or BNCT. CONCLUSION: These cases illustrate the ongoing challenges in differentiating between BNCT and chordoma. All had unique imaging features; three had atypical microscopic areas blending with BNCT or chordoma, strengthening the argument for a relationship between the two entities and supporting the idea that some BNCTs may progress to chordoma. Our study dispels the notion that any single radiologic criterion used to distinguish between chordoma and BNCT is reliable, opening the discussion as to whether or how to monitor BNCTs. |
format | Online Article Text |
id | pubmed-4212531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42125312014-10-30 Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them Kreshak, Jennifer Larousserie, Frédérique Picci, Piero Boriani, Stefano Mirra, Joseph Merlino, Biagio Brunocilla, Eugenio Vanel, Daniel Cancer Imaging Research Article BACKGROUND: Much discussion about benign notochordal cell tissue in vertebrae has centered on the nature of its relationship, if any, to chordoma. Often referred to as benign notochordal cell tumors (BNCTs), these lesions have unique morphological features, however, differentiating between notochordal cells in discs, BNCT, and chordoma can be difficult. They are described as radiologically distinct from chordoma, with lysis, contrast enhancement, and a soft tissue mass indicating chordoma. METHODS: All chordomas diagnosed at our institution, the Istituto Ortopedico Rizzoli (Bologna, Italy), prior to 2008 were reviewed, yielding 174 cases. Five were limited to bone; one was a recurrent chordoma without original data available. The remaining four were re-evaluated in detail. RESULTS: There were three women and one man, aged 33–57 years (mean, 48 years). Two were BNCTs and two were mixed lesions containing BNCT and chordoma. On computed tomography, all were radiopaque with areas of lysis. One BNCT was heterogeneous on magnetic resonance imaging, enhancing after contrast. Microscopically, one BNCT had a well-defined cystic area with a sclerotic border. The other had a minute atypical area; it recurred as chordoma. The mixed lesions had areas of definitive BNCT, definitive chordoma, and atypical areas that did not meet the criteria for either. The atypical areas in all three cases ‘blended’ with areas of chordoma or BNCT. CONCLUSION: These cases illustrate the ongoing challenges in differentiating between BNCT and chordoma. All had unique imaging features; three had atypical microscopic areas blending with BNCT or chordoma, strengthening the argument for a relationship between the two entities and supporting the idea that some BNCTs may progress to chordoma. Our study dispels the notion that any single radiologic criterion used to distinguish between chordoma and BNCT is reliable, opening the discussion as to whether or how to monitor BNCTs. BioMed Central 2014-04-22 /pmc/articles/PMC4212531/ /pubmed/25609192 http://dx.doi.org/10.1186/1470-7330-14-4 Text en Copyright © 2014 Kreshak et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kreshak, Jennifer Larousserie, Frédérique Picci, Piero Boriani, Stefano Mirra, Joseph Merlino, Biagio Brunocilla, Eugenio Vanel, Daniel Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title | Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title_full | Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title_fullStr | Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title_full_unstemmed | Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title_short | Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
title_sort | difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212531/ https://www.ncbi.nlm.nih.gov/pubmed/25609192 http://dx.doi.org/10.1186/1470-7330-14-4 |
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