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Indian Journal of Medical and Paediatric Oncology
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CASE REPORT AND REVIEW OF LITERATURE
Year : 2020  |  Volume : 41  |  Issue : 5  |  Page : 745-747

Long-term remission of metastatic pleomorphic paratesticular rhabdomyosarcoma with chemotherapy in an adolescent boy - A case report


1 Department of Pediatric Hematology and Oncology and Bone Marrow Transplantation, Health Care Global, Bengaluru, Karnataka, India
2 Department of Radiodiagnosis, Health Care Global, Bengaluru, Karnataka, India
3 Department of Surgical Oncology, Health Care Global, Bengaluru, Karnataka, India

Correspondence Address:
Dr. Intezar Mehdi
HCG Towers No. 8, Kalinga Rao Road, Sampangiram Nagar, Bengaluru - 560 095, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijmpo.ijmpo_85_20

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Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in the pediatric age group. They are classified based on the histopathological characteristics. The prognosis of RMS depends on the site of occurrence and the histopathology. Although paratesticular site is considered as one of the favorable sites, pleomorphic histology, even at this favorable site, confers a poor prognosis. Treatment includes surgery chemotherapy and radiation in metastatic cases. Here, we describe a case of an adolescent boy with pleomorphic paratesticular RMS treated successfully with chemotherapy.


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