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Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity

Teratocarcinosarcoma is a rare, highly aggressive malignancy of the head and neck, characterized by multiphenotypic and triphasic growth of epithelial, mesenchymal, and primitive neuroepithelial elements. Owing to its rarity and morphological heterogeneity, as well as the lack of experience with thi...

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Autor principal: AL-Zaidi, Rana S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515544/
https://www.ncbi.nlm.nih.gov/pubmed/37743905
http://dx.doi.org/10.1177/20363613231204047
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author AL-Zaidi, Rana S.
author_facet AL-Zaidi, Rana S.
author_sort AL-Zaidi, Rana S.
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description Teratocarcinosarcoma is a rare, highly aggressive malignancy of the head and neck, characterized by multiphenotypic and triphasic growth of epithelial, mesenchymal, and primitive neuroepithelial elements. Owing to its rarity and morphological heterogeneity, as well as the lack of experience with this neoplasm, teratocarcinosarcoma is often misdiagnosed, particularly in small biopsy samples when only some of the elements are identified, thus leading to delayed management. Aggressive clinical behavior and poor survival outcomes, necessitate an accurate diagnosis and appropriate treatment. This review describes the main demographic and clinicopathological features of teratocarcinosarcoma, with an emphasis on the recent advances that have attempted to identify the molecular signature of this neoplasm.
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spelling pubmed-105155442023-09-23 Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity AL-Zaidi, Rana S. Rare Tumors Review Teratocarcinosarcoma is a rare, highly aggressive malignancy of the head and neck, characterized by multiphenotypic and triphasic growth of epithelial, mesenchymal, and primitive neuroepithelial elements. Owing to its rarity and morphological heterogeneity, as well as the lack of experience with this neoplasm, teratocarcinosarcoma is often misdiagnosed, particularly in small biopsy samples when only some of the elements are identified, thus leading to delayed management. Aggressive clinical behavior and poor survival outcomes, necessitate an accurate diagnosis and appropriate treatment. This review describes the main demographic and clinicopathological features of teratocarcinosarcoma, with an emphasis on the recent advances that have attempted to identify the molecular signature of this neoplasm. SAGE Publications 2023-09-21 /pmc/articles/PMC10515544/ /pubmed/37743905 http://dx.doi.org/10.1177/20363613231204047 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
AL-Zaidi, Rana S.
Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title_full Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title_fullStr Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title_full_unstemmed Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title_short Teratocarcinosarcoma of the head and neck: Clinicopathologic review of a rare entity
title_sort teratocarcinosarcoma of the head and neck: clinicopathologic review of a rare entity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515544/
https://www.ncbi.nlm.nih.gov/pubmed/37743905
http://dx.doi.org/10.1177/20363613231204047
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