Review Article
Rhabdomyosarcoma: Advances in Molecular and Cellular Biology
Table 2
The histological types of rhabdomyosarcoma.
| Histological type | Predilection population | Predilection site | Risk category | Genetic change |
| ERMS | Infants or children under 10 years old | Head and neck region | Intermediate | LOH at chromosome 11p15.5 |
| ARMS | Adolescents and young adults | Deep tissue of extremity | High | t(2;13)(q35;q14); t(1;13)(p36;q14) |
| PRMS | Adult males | Throughout the body | High | JUN (1p31), MYC (8q24), CCND1 (11q13), INT2 (11q13.3), MDM2 (12q14.3–q15) |
| SRMS | In the first decade of life with a second mode centered around the fifth decade | The extremities, head, and neck | Superior | SRF-NCOA2; MYOD1 mutation |
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ERMS: embryonal rhabdomyosarcoma. ARMS: alveolar rhabdomyosarcoma. PRMS: pleomorphic rhabdomyosarcoma. SRMS: spindle cell/sclerosing rhabdomyosarcoma.
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