참고문헌
- Arndt CA, Stoner JA, Hawkins DS, et al (2009). Vincristine, Actinomycin and cyclophosphamide alternating with vincristine, topotecan and cyclophosphamide for intermediate risk rhabdomyosarcoma: children's oncology group study D9803. J ClinOncol, 27, 5182-8. https://doi.org/10.1200/JCO.2009.22.3768
- Bhurgri Y, Bhurgri A, Puri R, et al (2004). Rhabdomyosarcoma in Karachi 1998-2002. Asian Pac J Cancer Prev, 5, 284-90.
- Caillaud JM, et al (1989). Histopathologic classification of childhood rhabdomyosarcoma: a report from the international Society of Pediatric Oncology pathology panel. Med Pediatr Oncol, 17, 391-400. https://doi.org/10.1002/mpo.2950170508
- Cavazzana AO, et al (1992). Spindle cell rhabdomyosarcoma. A prognostically favourable variant of rhabdomyosarcoma. Am J Surg Pathol, 16, 229-35. https://doi.org/10.1097/00000478-199203000-00002
- Cessna MH, et al (2011). Are myogenin and Myo D1 expression specific for rhabdomyosarcoma? A study of 150 cases, with emphasis on spindle cell mimics. Am J Surg Pathol, 25, 1150-7.
- Chiles MC, Parhaw DM, Qualman SJ, et al (2004). Sclerosing rhabdomyosarcoma in children and adolescents: a clinicopathologic review of 13 cases from the intergroup rhabdomyosarcoma study group and children's oncology group. Pediatr Dev Pathol, 7, 583-94. https://doi.org/10.1007/s10024-004-5058-x
- Gurney JG, Davis S, Severson RK, et al (1996). Trends in cancer incidence among children in the U.S. Cancer, 78, 532-41. https://doi.org/10.1002/(SICI)1097-0142(19960801)78:3<532::AID-CNCR22>3.0.CO;2-Z
- Gurney JG, Ross JA, Wall DA, et al (1997). Infant cancer in the U.S. histology specific incidence and trends, 1973 to 1992. J Pediatr Hematol Oncol, 19, 428-32. https://doi.org/10.1097/00043426-199709000-00004
- Harms D (1995). Alveolar rhabdomyosarcoma: a prognostically unfavourable rhabdomyosarcoma type and its necessary distinction from embryonal rhabdomyosarcoma. Curr Top Pathol, 89, 273-96. https://doi.org/10.1007/978-3-642-77289-4_14
- Hawkins WG, Hoos A, Antonescu CR, et al (2001). Clinicopathologic analysis of patients with adult rhabdomyosarcoma. Cancer, 91, 794-803. https://doi.org/10.1002/1097-0142(20010215)91:4<794::AID-CNCR1066>3.0.CO;2-Q
- Jo VY, Marino-Enriquez A, Flethcher CD (2011). Epithelioid rhabdomyosarcoma; clinicopathologic analysis of 16 cases of a morphologically distinct variant of rhabdomyosarcoma. Am J Surg Pathol, 35, 1523-30. https://doi.org/10.1097/PAS.0b013e31822e0907
- Joshi D anderson JR, et al (2004). Age is an independent prognostic factor in rhabdomyosarcoma: a report from the soft tissue sarcoma committee of the children's oncology group. Pediatr Blood Cancer, 42, 64-73. https://doi.org/10.1002/pbc.10441
- Liu CX, et al (2014). Compound HRAS/PIK3CA mutations in Chinese patients with alveolar rhabdomyosarcoma. Asian Pac J Cancer Prev, 15, 1771-4. https://doi.org/10.7314/APJCP.2014.15.4.1771
- Meyer WH, Spunt SL (2004). Soft tissue sarcomas of childhood. Cancer Treat Rev, 30, 269-80. https://doi.org/10.1016/j.ctrv.2003.11.001
- Missaoni N, et al (2010). Pediatric rhabdomyosarcoma in Tunisia. Asian Pac J Cancer Prev, 11, 1325-7.
- Molenaar WM, Oosterhuis JW, Oosterhuis AM, Ramaekers FC (1985). Mesenchymal and muscle specific intermediate filaments (vimentin and desmin) in relation to differentiation in childhood rhabdomyosarcoma. Hum Pathol, 16, 838-43. https://doi.org/10.1016/S0046-8177(85)80256-2
- Morotti RA, et al (2006). An immunhistochemical algorithm to facilitate diagnosis and subtyping of rhabdomyosarcoma; the children's oncology group experience. Am J Surg Pathol, 30, 962-8. https://doi.org/10.1097/00000478-200608000-00005
- Newton Jr WA, et al (1995). Classification of rhabdomyosarcomas and related sarcomas. Prognostic aspects and proposal for a new classification-an intergroup rhabdomyosarcoma study. Cancer, 76, 1073-85. https://doi.org/10.1002/1097-0142(19950915)76:6<1073::AID-CNCR2820760624>3.0.CO;2-L
- Ognjanovic S, Linabery AM, Charbonneau B, Ross JA (2009). Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975-2005. Cancer, 115, 4218-26. https://doi.org/10.1002/cncr.24465
- Parkin DM, Stiller CA, Drager GJ, Bieber CA (1988).The international incidence of childhood cancer. Int J Cancer, 42, 511-20. https://doi.org/10.1002/ijc.2910420408
- Raney RB, Walterhouse DO, Meza JL, et al (2011). Results of the intergroup rhabdomyosarcoma study group D9602 protocol, using vincristine and dactinomysin with or without cyclophosphamide and radiation therapy, for newly diagnosed patients with low risk embryonal rhabdomyosarcoma: a report from the soft tissue sarcoma committee of the children's oncology group. J Clin Oncol, 29, 1312-8. https://doi.org/10.1200/JCO.2010.30.4469
- Stock N, et al (2009). Adult-type rhabdomyosarcoma:analysis of 57 cases with clinicopathologic description, identification of 3 morphologic patterns and prognosis. Am J Surg Pathol, 33, 1850-9. https://doi.org/10.1097/PAS.0b013e3181be6209
- Sultan I, Qaddonmi I, Yaser S, Rodrigue-Galindo C, Ferrari A (2009). Comparing adult and pediatricrhabdomyosarcoma in the surveillance, epidemiology and end results program, 1973 to 2005: an analysis of 2600 patients. J Clin Oncol, 27, 3391-7. https://doi.org/10.1200/JCO.2008.19.7483
- WHO Classification of Tumors of Soft Tissue and Bone (2013). Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F eds. 4th Edition. International Agency for Research on Cancer (IARC), Lyon, 123-36.
- Yasuda T, et al (2009). Alveolar rhabdomyosarcoma of the head and neck region in older adults: genetic characterization and review of the literature. Human Pathol, 40, 341-8. https://doi.org/10.1016/j.humpath.2008.08.006