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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...

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Dades bibliogràfiques
Publicat a:Avicenna J Med
Autors principals: Ahmad, Tagrid Younes, Al Houri, Hasan Nabil, Al Houri, Abdullah Nabil, Ahmad, Nagham Younes
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2018
Matèries:
Accés en línia: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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