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Head and Neck Rhabdomyosarcoma Harboring TFCP2 Fusions and ALK overexpression: A Clinicopathologic and Molecular Analysis of 11 cases
BACKGROUND: Primary intraosseous rhabdomyosarcoma (RMS) is a rare entity defined by EWSR1/FUS-TFCP2 or less commonly MEIS1-NCOA2 fusions. The lesions often display a hybrid spindle and epithelioid phenotype, frequently co-express myogenic markers, ALK and cytokeratin, and show a striking propensity...
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| Publicado no: | Histopathology |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8243398/ https://ncbi.nlm.nih.gov/pubmed/33382123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/his.14323 |
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