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...
Guardado en:
Autores principales: | Tagrid Younes Ahmad, Hasan Nabil Al Houri, Abdullah Nabil Al Houri, Nagham Younes Ahmad |
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Formato: | article |
Lenguaje: | EN |
Publicado: |
Thieme Medical and Scientific Publishers Pvt. Ltd.
2018
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Materias: | |
Acceso en línea: | https://doaj.org/article/6ae093a9272f413bae66f433c7be28a5 |
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