Department of Pathology, Rush University Medical Center, Chicago, IL 60612, USA.
Arch Pathol Lab Med. 2010 Aug;134(8):1210-4. doi: 10.5858/2009-0464-CR.1.
The solid variant of papillary renal cell carcinoma, when strictly defined as a tumor in which no true papillae can be identified, is extremely rare, with only a few cases reported in the literature. This tumor is characterized histologically by solid sheets of cells without true papillae; nevertheless, immunohistochemical and genetic analysis supports the classification of this tumor as a variant of papillary renal cell carcinoma. We report a case of solid variant of papillary renal cell carcinoma affecting a young man and provide histologic and clinical follow-up data, adding an additional case of this extremely rare pathology to the literature. In addition, we describe the first case, to our knowledge, of a solid variant of papillary renal cell carcinoma to contain a high-grade (sarcomatoid) spindle cell component.
实性乳头状肾细胞癌,当严格定义为肿瘤中无法识别真正乳头时,极为罕见,文献中仅报道了少数几例。该肿瘤组织学上表现为实性片状细胞,无真正乳头;然而,免疫组化和遗传学分析支持将该肿瘤归类为乳头状肾细胞癌的一种变体。我们报告了一例影响年轻男性的实性乳头状肾细胞癌,并提供了组织学和临床随访数据,为该罕见病变的文献再添一例。此外,据我们所知,我们首次描述了含有高级别(梭形细胞)成分的实性乳头状肾细胞癌病例。