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¿µ³²ÀÇ´ëÇмúÁö Vol.28 No.1 p70-76, June2011

Case Report

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Paratesticular Alveolar Rhabdomyosarcoma with Multiple Lymph Nodes Metastasis Successfully Treated with Chemotherapy

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Tel: (053) 620-3830, Fax: (053) 654-8386
E-mail : hms@med.yu.ac.kr

June 30, 2011

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.

Key Words: Rhabdomyosarcoma, Alveolar, Lymphatic Metastasis

References

1. Pappo AS, Shapiro DN, Crist WM. Rhabdo- myosarcoma. Biology and treatment. Pediatr Clin North Am 1997;44:953-72.

2. DeVita V, Lawrence T, DePinho R, Weinberg R. DeVita, Hellman, and Rosenberg's Cancer Principles & Practice of Oncology. In: HeiDi V, Alberto S, Jed G. Solid Tumors of Childhood. 8th ed. philadelphia, Lippincott Williams and Wikins Press; 2008. p. 2068-70.

3. Dagher R, Helman L. Rhabdomyosarcoma: an overview. Oncologist 1999;4:34-44.

4. Crist W, Gehan EA, Ragab AH, Dickman PS, Donaldson SS, Fryer C, et al. The Third Intergroup Rhabdomyosarcoma Study. J Clin Oncol 1995;13:610-30.

5. Meyer WH, Spunt SL. Soft tissue sarcomas of childhood. Cancer Treat Rev 2004;30:269-80.

6. Maurer HM, Beltangady M, Gehan EA, Crist W, Hammond D, Hays DM, et al. The intergroup rhabdomyosarcoma study-I. a final report. Cancer 1988:61;209-20.

7. Maurer HM, Gehan EA, Beltangady M, Crist W, Dickman PS, Donaldson SS, et al. The intergroup rhabdomyosarcoma study-II. Cancer 1993;71:1904-22.

8. Crist WM, Anderson JR, Meza JL, Fryer C, Raney RB, Ruymann FB, et al. Intergroup rhabdomyosarcoma study-IV: results for patients with nonmetastatic disease. J Clin Oncol 2001; 19:3091-102.

9. Koscielniak E, Harms D, Henze G, Jurgens H, Gadner H, Herbst M, et al. 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 1999;17:3706-19.

10. Jong AS, van Vark M, Albus-Lutter CE, van Raamsdonk W, Voute PA. Myosin and myoglobin as tumor markers in the diagnosis of rhabdomyosarcoma. a comparative study. Am J Surg Pathol 1984;8:521-8.

11. Raney RB, Maurer HM, Anderson JR, Andrassy RJ, Donaldson SS, Qualman SJ, et al. 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 2001;5:9-15.

12. Miser JS, Kinsella TJ, Triche TJ, Tsokos M, Jarosinski P, Forquer R, et al. 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 1987;5:1191-8.

13. Ferrari A, Dileo P, Casanova M, Bertulli R, Meazza C, Gandola L, et al. Rhabdomyosarcoma in adults. A retrospective analysis of 171 patients treated at a single institution. Cancer 2003;98:571-80.

14. Raney RB, Anderson JR, Barr FG, Donaldson SS, Pappo AS, Qualman SJ, et al. 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 2001;23:215-20.