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DOI: 10.1055/s-0038-1633759
A Case of Orbital Rhabdomyosarcoma in Adult
Autoren
Rhabdomyosarcoma (RMS) is a highly malignant tumor in which the tissue of origin is pluripotent mesenchyme. It is the most common soft tissue sarcoma of the head and neck in childhood and comprises 4% of all pediatric malignancies, with 10% of all cases occurring in the orbit. Most of RMS occur in the first decade of life; however, it has been reported from birth to the eighth decade. Recently, we experienced a rare case of a 33-year-old man with orbital RMS; therefore, we present this case with a review of literature.
Publikationsverlauf
Publikationsdatum:
02. Februar 2018 (online)
© 2018. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
