Primary renal synovial sarcoma
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Girish D. Bakhshi
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gdbakhshi@yahoo.com
Department of Surgery, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
- Arshad S. Khan Department of Surgery, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
- Aftab S. Shaikh Department of Surgery, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
- Mohammad Ashraf A. Khan Department of Surgery, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
- Mohammad Adil A. Khan Department of Surgery, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
- Nilofar M. Jamadar Department of Radiology, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
Abstract
Primary Renal Sarcoma is rare tumor comprising only 1% of all renal tumours. Synovial sarcomas are generally deep-seated tumors arising in the proximity of large joints of adolescents and young adults and account for 5-10% of all soft tissue tumours. Primary synovial sarcoma of kidney is rare and has poor prognosis. It can only be diagnosed by immunohistochemistry. It should be considered as a differential in sarcomatoid and spindle cell tumours. We present a case of 33-year-old female, who underwent left sided radical nephrectomy for renal tumour. Histopathology and genetic analysis diagnosed it to be primary renal synovial sarcoma. Patient underwent radiation therapy and 2 years follow up is uneventful. A brief case report with review of literature is presented.Downloads
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Published
2012-03-30
Issue
Section
Case Reports
Keywords:
renal tumor, synovial sarcoma.
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How to Cite
Bakhshi, G., Khan, A., Shaikh, A., Khan, M. A., Khan, M. A., & Jamadar, N. (2012). Primary renal synovial sarcoma. Clinics and Practice, 2(2), e44. https://doi.org/10.4081/cp.2012.e44
Copyright (c) 2012 Girish D. Bakhshi, Arshad S. Khan, Aftab S. Shaikh, Mohammad Ashraf A. Khan, Mohammad Adil A. Khan, Nilofar M. Jamadar
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
