Title of article :
A 8-year survivor of unresectable intrapelvic desmoplastic small round cell tumor treated with concurrent chemoradiotherapy
Author/Authors :
Saitoh, J.I. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Ishikawa, H. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Ebara, T. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Katoh, H. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Ohno, T. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Takahashi, T. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan , Akimoto, T. Tokyo Women’s Medical University - Department of Radiology, Japan , Nakajima, T. Shizuoka Cancer Center - Department of Pathology, Japan , Nakano, T. Gunma University Graduate - School of Medicine - Department of Radiation Oncology, Japan
From page :
201
To page :
205
Abstract :
Desmoplastic small round cell tumor is a rare malignant tumor that occurs primarily in young males. Here, a case of small round cell tumor in an adult male successfully treated with a curative concurrent chemoradiotherapy is presented. A 58-year-old man had an intrapelvic tumor. Surgical resection was attempted, but the tumor was unresectable. Needle biopsy was performed and the diagnosis was suggested to be desmoplastic small round cell tumor. Concurrent chemoradiotherapy was performed, and a complete response was obtained. This patient has been alive for 8 years after treatment with no evidence of disease. Concurrent chemoradiotherapy appears to be a useful treatment choice for unresectable desmoplastic small round cell tumor.
Keywords :
desmoplastic small round cell tumor , concurrent chemoradiotherapy , retroperitoneum
Journal title :
International Journal of Radiation Research
Journal title :
International Journal of Radiation Research
Record number :
2666510
Link To Document :
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