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Familial chordoma: A case report and review of the literature
Familial skull base chordoma is a rare tumor derived from the remnants of the embryonic notochord. The present study describes the clinical presentation of 4 cases of skull base chordomas in a family. A 15-year-old female received staged surgeries and was pathologically confirmed with a diagnosis of...
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| Pubblicato in: | Oncol Lett |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
D.A. Spandidos
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4665336/ https://ncbi.nlm.nih.gov/pubmed/26722267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.3687 |
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