전이성 고환주위 폐포성 횡문근육종 1예
Paratesticular Alveolar Rhabdomyosarcoma with Multiple Lymph Nodes Metastasis Successfully Treated with Chemotherapy
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초록
Rhabdomyosarcomas are soft tissue sarcomas; while extremely rare in adults, they are one of the most common neoplasms in children and adolescents. Histologically, they can be classified into embryonal(ERMS), alveolar(ARMS), pleomorphic, and undifferentiated types. The ARMS type is very rare, and is associated with a poor prognosis. Common primary sites of ARMS are the trunk and extremities. We report on a case of paraaortic, supraclavicular, and axillary lymph node metastasis from paratesticular ARMS treated with VAC(vincristine, dactinomycin, cyclophosphamide)/IE(ifosfamide, etoposide) chemotherapy in a young adult. Administration of six cycles of chemotherapy with VAC/IE resulted in complete remission. The patient has maintained complete remission over the past 27 months.
Abstract
Rhabdomyosarcomas are soft tissue sarcomas; while extremely rare in adults, they are one of the most common neoplasms in children and adolescents. Histologically, they can be classified into embryonal(ERMS), alveolar(ARMS), pleomorphic, and undifferentiated types. The ARMS type is very rare, and is associated with a poor prognosis. Common primary sites of ARMS are the trunk and extremities. We report on a case of paraaortic, supraclavicular, and axillary lymph node metastasis from paratesticular ARMS treated with VAC(vincristine, dactinomycin, cyclophosphamide)/IE(ifosfamide, etoposide) chemotherapy in a young adult. Administration of six cycles of chemotherapy with VAC/IE resulted in complete remission. The patient has maintained complete remission over the past 27 months.
참고문헌 (14)
- Pappo AS, "Rhabdo- myosarcoma. Biology and treatment", Pediatr Clin North Am, 44, pp.953~972 (1997)
- DeVita V, "Solid Tumors of Childhood", pp.2068~2070 (2008), Lippincott Williams and Wikins Press
- Dagher R, "Rhabdomyosarcoma: an overview", Oncologist, 4, pp.34~44 (1999)
- Crist W, "The Third Intergroup Rhabdomyosarcoma Study", J Clin Oncol, 13, pp.610~630 (1995)
- Meyer WH, "Soft tissue sarcomas of childhood", Cancer Treat Rev, 30, pp.269~280 (2004)
- Maurer HM, "The intergroup rhabdomyosarcoma study-I. a final report", Cancer, 61, pp.209~220 (1988)
- Maurer HM, "The intergroup rhabdomyosarcoma study-II", Cancer, 71, pp.1904~1922 (1993)
- Crist WM, "Intergroup rhabdomyosarcoma study-IV : results for patients with nonmetastatic disease", J Clin Oncol, 19, pp.3091~3102 (2001)
- Koscielniak E, "Results of treatment for soft tissue sarcoma in childhood and adolescence: a final report of the german cooperative soft tissue sarcoma study CWS- 86", J Clin Oncol, 17, pp.3706~3719 (1999)
- Jong AS, "Myosin and myoglobin as tumor markers in the diagnosis of rhabdomyosarcoma. a comparative study", Am J Surg Pathol, 8, pp.521~528 (1984)
- Raney RB, "The intergroup rhabdomyosarcoma study group (IRSG): major lessons from the IRS-I through IRS-IV studies as background for the current IRS-V treatment protocols", Sarcoma, 5, pp.9~15 (2001)
- Miser JS, "Ifosfamide with mesna uroprotection and etoposide: an effective regimen in the treatment of recurrent sarcomas and other tumors of children and young adults", J Clin Oncol, 5, pp.1191~1198 (1987)
- Ferrari A, "Rhabdomyosarcoma in adults. A retrospective analysis of 171 patients treated at a single institution", Cancer, 98, pp.571~580 (2003)
- Raney RB, "Rhabdo- myosarcoma and undifferentiated sarcoma in the first two decades of life: a selective review of intergroup rhabdomyosarcoma study group experience and rationale for intergroup rhabdomyosarcoma study V", J Pediatr Hematol Oncol, 23, pp.215~220 (2001)
