BCOR Overexpression in Renal Malignant Solitary Fibrous Tumors A Close Mimic of Clear Cell Sarcoma of Kidney

被引:27
|
作者
Argani, Pedram [1 ,2 ]
Kao, Yu-Chien [3 ]
Zhang, Lei [4 ]
Sung, Yun-Shao [4 ]
Alaggio, Rita [5 ]
Swanson, David [6 ]
Matoso, Andres [1 ,2 ]
Dickson, Brendan C. [6 ]
Antonescu, Cristina R. [4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[3] Taipei Med Univ, Dept Pathol, Shuang Ho Hosp, Taipei, Taiwan
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[5] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA
[6] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON, Canada
关键词
renal neoplasm; solitary fibrous tumor; BCOR; translocation; INTERNAL TANDEM DUPLICATIONS; GENE FUSION; EXPRESSION; METASTASIS; VARIANTS; BENIGN; TISSUE;
D O I
10.1097/PAS.0000000000001243
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BCOR immunoreactivity is a sensitive and highly specific marker for clear cell sarcoma of the kidney (CCSK). However, a subset of adult renal sarcomas which overexpress BCOR are negative for BCOR genetic alterations, including BCOR gene fusions or BCOR-internal tandem duplication, and thus remain unclassified. We report 5 such undifferentiated renal/perirenal sarcomas which raised the differential diagnosis of CCSK due to their morphologic appearance and strong BCOR immunoreactivity, but which on RNA sequencing proved to be malignant solitary fibrous tumors (SFTs). The neoplasms occurred in patients at an age range of 30 to 62 years. Three patients were females and 2 male. Four were primary renal neoplasms while one was perirenal. All 5 neoplasms were cellular, nonpleomorphic, undifferentiated sarcomas with branching capillary vasculature composed of primitive round to ovoid neoplastic cells with scant cytoplasm and nuclei having fine, evenly dispersed chromatin. None of the cases demonstrated the typical hyperchromatic fusiform nuclei, prominent collagen deposition, or hemangiopericytomatous vasculature of SFT. All 5 cases were strongly immunoreactive for BCOR. Three cases were CD34 negative, where the other 2 were only focally CD34 positive. STAT6 was subsequently found to be positive by immunohistochemistry in all 5 cases. In summary, we report a previously unrecognized mimic of CCSK: malignant SFTs with an undifferentiated/small round cell phenotype along with branching capillary vasculature, strong im-munoreactivity for BCOR, and minimal or no immunoreactivity for CD34. As CCSK is treated with a specific chemotherapy regimen, this distinction has therapeutic implications.
引用
收藏
页码:773 / 782
页数:10
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