Ashida S, Yamamoto A, Fukumori T, Yuasa K, Terao N, Iwata J
Department of Urology, Kochi Takasu Hospital.
Hinyokika Kiyo. 1997 Nov;43(11):777-80.
We report a case of chromophobe cell renal carcinoma. A 59-year-old female was admitted to our hospital with asymptomatic gross hematuria. Abdominal computerized tomography showed an approximately 4 cm. minimally enhancing mass in the left kidney. Angiography revealed a hypovascular tumor in the left kidney. Under the diagnosis of renal cell carcinoma, left radical nephrectomy was performed. The cut surface of the tumor was beige in color with few foci of hemorrhage and necrosis. Microscopically, the tumor was composed of the cells with voluminous reticulated cytoplasm stained lightly with routine hematoxylin and eosin. Hale's colloidal iron staining demonstrated a positive cytoplasmic reaction. Pathological diagnosis was chromophobe cell renal carcinoma. Chromophobe cell renal carcinoma is a recently established subtype of renal cell carcinoma, which has rarely been reported in Japan.
我们报告一例嫌色细胞肾细胞癌。一名59岁女性因无症状肉眼血尿入住我院。腹部计算机断层扫描显示左肾有一个约4厘米的轻度强化肿块。血管造影显示左肾有一个少血管肿瘤。在诊断为肾细胞癌后,进行了左肾根治性切除术。肿瘤切面呈米色,有少量出血和坏死灶。显微镜下,肿瘤由细胞质丰富、呈网状、常规苏木精和伊红染色浅的细胞组成。黑尔胶体铁染色显示细胞质呈阳性反应。病理诊断为嫌色细胞肾细胞癌。嫌色细胞肾细胞癌是最近确立的肾细胞癌亚型,在日本鲜有报道。