A case of primary renal angiosarcoma

Author:

Yoshida Kazuhiko1,Ito Fumio1,Nakazawa Hayakazu1,Maeda Yoshiko1,Tomoe Hikaru1,Aiba Motohiko2

Affiliation:

1. Department of Urology, Tokyo Women's Medical University Medical Center East, Nishiogu, Arakawa-ku, Tokyo, Japan

2. Department of Surgical Pathology, Tokyo Women's Medical University Medical Center East, Nishiogu, Arakawa-ku, Tokyo, Japan

Abstract

A 78-year old man was diagnosed with a left bleeding renal cyst from CT scan results. Serial CT scans revealed the left kidney mass to be increasing in size and a new lesion in the liver. Renal cell carcinoma with liver metastasis was diagnosed and a radical nephrectomy performed. The initial pathological diagnosis was a benign chronic hematoma. However, the liver mass increased in size and multiplied, while another mass emerged in the twelfth thoracic vertebra with spinal paralysis and was immediately removed. Pathological findings for that specimen showed malignancy of stromal cell origin but low atypia. The renal specimen was re-evaluated using whole cross-section analysis and immunohistochemistry, and diagnosed as a primary renal angiosarcoma. Recombinant interleukin-2 therapy was started immediately; however, the patient died of metastatic disease 13 months after the initial operation. Although contrast imaging depicted the primary lesion as a non-specific hematoma with little focal pooling, and low-grade cytological atypia was shown pathologically, the angiosarcoma was extremely aggressive.

Publisher

SAGE Publications

Subject

Oncology,Histology

Reference10 articles.

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