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Aggressive orbital rhabdomyosarcoma in adulthood: A case report in a public hospital in Damascus, Syria
Orbital rhabdomyosarcoma (RMS) is a highly malignant tumor that originates mainly from mesenchymal tissue. It is considered a rare childhood malignancy; therefore, presentation in adulthood is scarce. In this case report, a 36-year-old male patient presented with a rapidly progressive RMS of the lef...
Uloženo v:
| Vydáno v: | Avicenna J Med |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6057160/ https://ncbi.nlm.nih.gov/pubmed/30090751 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ajm.AJM_62_18 |
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