期刊论文详细信息
Diagnostic Pathology
Mucinous tubular and spindle cell carcinoma and solid variant papillary renal cell carcinoma: a clinicopathologic comparative analysis of four cases with similar molecular genetics datum
Donghong Yu1  Shiwu Wu1  Qiong Zhang1  Xiaoli Wang1  Qiong Wu1  Xiang Yong1  Yanling Zhang1 
[1] Department of Pathology, the Frist Affiliated Hospital of Bengbu Medical College, 287 Changhuai Road, Bengbu, 233000, Anhui, PR China
关键词: Immunohistochemistry;    Fluorescence in situ hybridization;    Mucinous tubular and spindle cell carcinoma;    Renal cell;    Carcinoma;   
Others  :  1149175
DOI  :  10.1186/s13000-014-0194-8
 received in 2014-08-09, accepted in 2014-10-07,  发布年份 2014
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【 摘 要 】

Mucinous tubular and spindle cell carcinoma (MTSC) was first recognized as a specific entity in the World Health Organization 2004 classification. The “classic” tumor presentation includes an extracellular blue-gray mucinous/myxoid matrix accompanying the typical tubular and spindle cell epithelial components. Tubules are lined by cuboidal to columnar cells with bland nuclei, central small to medium sized nucleoli, and few to no mitoses. By expanding the histologic spectrum, a number of studies highlighted the distinction between MTSC and solid variant of papillary renal cell carcinoma (sPRCC), although controversy still exists. Here, we evaluated two cases of MTSC and compared two cases of sPRCC by light microscopy, special staining, immunohistochemical staining and fluorescence in situ hybridization (FISH). We found that morphologic and immunophenotyping features showed more overlap between MTSC and sPRCC. In addition, gains of chromosomes 7 and 17 and loss of Y, which are characteristic of PRCC, were observed in two cases of sPRCC and one case of MTSC, suggesting that MTSC is similar to sPRCC or may be a subtype of PRCC.

Virtual Slides: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_194 webcite

【 授权许可】

   
2014 Zhang et al.; licensee BioMed Central Ltd.

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