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RESIDENT’S CORNER

Renal angiosarcoma: a case report and literature review

Tsu-Yee Joseph Lee1, Joseph Lawen2, Rekha Gupta1

1 Department of Pathology, QEII Health Science Center, Dalhousie University, Halifax, Nova Scotia, Canada
2 Department of Urology, QEII Health Science Center, Dalhousie University, Halifax, Nova Scotia, Canada
Address correspondence to Dr. R Gupta, Department of Pathology, Dalhousie University, Room 725, 7th Floor DJ Mackenzie Building, 5788 University Avenue, Halifax, Nova Scotia B3H 2Y9 Canada

Canadian Journal of Urology 2007, 14(1), 3471-3476.

Abstract

Purpose: In adults renal cell carcinoma (RCC) accounts for over 85% of all diagnosed renal cancers. A much more rare and aggressive malignant tumor of the kidney is angiosarcoma (AS) with less than 25 cases described internationally. Both RCC and AS have similar radiological appearances and thus require histological evaluation for definitive diagnosis. We present a case of renal AS in a 63-year old male who was initially radiologically diagnosed as RCC, and review the current renal AS literature.
Methods: The current English literature from 1981 and onwards on renal AS was reviewed and compared to our current case.
Results: The median age and sex of patients with renal AS at presentation was 63 years old (mean 61 years) and common in males with a left kidney predominance. Symptoms included flank pain, palpable mass, and hematuria with imaging suggestive of RCC. Hematogenous metastatic spread often occurred with median survival time of 3.5 months from time of diagnosis (mean 5.8 months). Histologically, the tumors have classical features of angiosarcoma with numerous blood-filled vascular spaces lined by plump pleomorphic endothelial cells with CD31 and CD34 staining positivity. Overall treatment was radical nephrectomy with radiation therapy for local control and metastases. The use of chemotherapy was not consistent.
Conclusion: Although RCC accounts for the majority of malignant renal tumors, the poor prognosis of AS and its similar radiological appearance to RCC imparts the importance of histological evaluation and the potential radiological mimicry of AS.

Keywords

renal cell carcinoma, renal angiosarcoma

Cite This Article

APA Style
Lee, T.J., Lawen, J., Gupta, R. (2007). Renal angiosarcoma: a case report and literature review. Canadian Journal of Urology, 14(1), 3471–3476.
Vancouver Style
Lee TJ, Lawen J, Gupta R. Renal angiosarcoma: a case report and literature review. Can J Urology. 2007;14(1):3471–3476.
IEEE Style
T.J. Lee, J. Lawen, and R. Gupta, “Renal angiosarcoma: a case report and literature review,” Can. J. Urology, vol. 14, no. 1, pp. 3471–3476, 2007.



cc Copyright © 2007 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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