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KMT2C mutation is a diagnostic molecular marker for primary thyroid osteosarcoma: A case report and literature review
Primary thyroid osteosarcoma is an extremely rare tumor which is associated with a poor prognosis. In this study, we describe an additional case. A 4.5 × 3.8 cm irregular heterogeneous nodule was examined in the left thyroid gland of a 72-year-old woman. Cytological smears and histopathological spec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679279/ https://www.ncbi.nlm.nih.gov/pubmed/36425109 http://dx.doi.org/10.3389/fmed.2022.1030888 |