Department of Diagnostic Radiology, Institute of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 7340037, Japan.
Department of Diagnostic Radiology, National Hospital Organization Kure Medical Center, 3-1 Aoyama-cho, Kure, Hiroshima, 7370023, Japan.
Jpn J Radiol. 2016 Apr;34(4):307-11. doi: 10.1007/s11604-016-0525-7. Epub 2016 Feb 1.
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.
肾管状囊性癌罕见且通常呈惰性。我们的病例涉及侵袭性管状囊性癌,并通过影像学证实其与乳头状肾细胞癌有关。一名 46 岁男性因肾多房性囊肿伴实性部分就诊。在计算机断层扫描和磁共振成像上,实性部分表现出乳头状肾细胞癌的特征。由于囊肿的存在,实性部分的增强呈絮状稀疏。肾周脂肪侵犯导致外生性囊肿,肾门部囊性淋巴结转移存在。组织病理学诊断为管状囊性癌伴乳头状肾细胞癌和低分化癌转移。我们的病例提示管状囊性癌的实性部分增强倾向于呈絮状稀疏,外生性囊肿和囊性淋巴结可能表现出影像学侵袭性表现。