Low‐grade renal cell carcinoma arising from the lower nephron: A case report with immunohistochemical, histochemical and ultrastructural studies
Low‐grade renal cell carcinoma arising from the lower nephron: A case report with immunohistochemical, histochemical and ultrastructural studies
复制标题
源自下肾单位的低度肾细胞癌:免疫组织化学、组织化学和超微结构研究的病例报告
DOI:
10.1046/j.1440-1827.2001.01297.x
复制
发表时间:
2001
影响因子:
2.2
通讯作者:
Y. Nagashima
中科院分区:
文献类型:
--
作者:
M. Otani;Tohru Shimizu;H. Serizawa;Y. Ebihara;Y. Nagashima
Most renal cell carcinomas (RCC) are composed of clear cells with sinusoid‐like vasculatures and originate from the proximal tubule. On the other hand, collecting duct carcinoma (CDC) and chromophobe RCC are thought to originate from the lower nephron. In the present study, we present a case of unusual RCC. The patient was a 68‐year‐old Japanese woman who had developed general fatigue with hematuria. Computed tomography revealed a left renal tumor suggesting sarcoma. The resected tumor was located in the renal parenchyma, measuring 12 × 10 × 8 cm in size. Histologically, the tumor consisted principally of cuboidal cells forming parallel or radiating arrays, continuous with the spindle‐shaped cells. Most parts of the tumor showed hemorrhagic necrosis. Immunohistochemically, tumor cells were positive for high molecular weight cytokeratins, vinculin, vimentin, CD15 and epithelial membrane antigen, and showed affinities with some kinds of lectins. N‐ and E‐cadherins and β‐catenin were diffusely positive in tumor cells. Nuclear positivity for Ki‐67 and p53 protein were approximately 2.0 and 1.7%, respectively. Considering its morphological and histochemical natures, this tumor is considered to have originated from the lower nephron, which is unique for a tumor of low‐grade malignancy.