Embryonal rhabdomyosarcomaembryonal rhabdomyosarcoma, embryonal rhabdomyosarcoma survival rate
Embryonal rhabdomyosarcoma ERMS is a rare histological form of cancer of connective tissue wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo It is the most common soft tissue sarcoma occurring in children1
ERMS is the more common of two major subtypes of rhabdomyosarcoma, the other being alveolar rhabdomyosarcoma
It has been informally classified as a "small round blue cell tumor"1 because of the characteristic microscopic appearance of its cells after histological staining with hematoxylin and eosin
Prognosis and survivaledit
The prognosis for rhabdomyosarcoma has improved greatly in recent decades, with over 70% of patients surviving for five years after diagnosis2
- ^ a b Masola V, Maran C, Tassone E, Zin A, Rosolen A, Onisto M 2009 "Heparanase activity in alveolar and embryonal rhabdomyosarcoma: implications for tumor invasion" BMC Cancer 9: 304 PMC 2743710 PMID 19715595 doi:101186/1471-2407-9-304
- ^ Breitfeld PP, Meyer WH August 2005 "Rhabdomyosarcoma: new windows of opportunity" Oncologist 10 7: 518–27 PMID 16079319 doi:101634/theoncologist10-7-518
|Not otherwise specified||
|Connective tissue neoplasm||
|Complex mixed and stromal||
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