A case of tubulocystic carcinoma of the kidney with aggressive features

Springer Science and Business Media LLC - Tập 34 - Trang 307-311 - 2016
Yoko Maeda1,2, Keisuke Goto3,4, Yukiko Honda1, Naoto Kuroda5, Kazuhiro Sentani3, Wataru Yasui3, Tetsutaro Hayashi4, Jun Teishima4, Akio Matsubara4, Yuko Nakamura1,6, Naoyuki Toyota2, Makoto Iida1, Kazuo Awai1
1Department of Diagnostic Radiology, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan
2Department of Diagnostic Radiology, National Hospital Organization Kure Medical Center, Hiroshima, Japan
3Department of Molecular Pathology, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan
4Department of Urology, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan
5Department of Diagnostic Pathology, Kochi Red Cross Hospital, Kochi, Japan
6Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, USA

Tóm tắt

Tubulocystic carcinoma of the kidney is rare and typically indolent. Our case involved an aggressive tubulocystic carcinoma as well as the radiological confirmation of its relation to papillary renal cell carcinoma. A 46-year-old male presented with renal multiloculated cysts with a solid part. On computed tomography and magnetic resonance imaging, the solid part showed the characteristics of papillary renal cell carcinoma. Contrast enhancement of the solid part was fluffy and sparse because of the coexistence of cysts. Perirenal fat invasion resulted in exophytic cysts, and renal-hilar cystic lymph node metastasis existed. The histopathological diagnosis was tubulocystic carcinoma associated with areas of papillary renal cell carcinoma and poorly differentiated carcinoma with metastasis. Our case suggests that the solid part enhancement of tubulocystic carcinoma tends to be fluffy and sparse, and exophytic cysts and cystic lymph nodes may show radiologically aggressive findings.

Tài liệu tham khảo

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