Desmoplastic small round cell tumor: RT-PCR analysis and immunohistochemical detection of the Wilm's tumor gene WT1

被引:16
作者
Barnoud, R
Delattre, O
Peoc'h, M
Pasquier, D
Plantaz, D
Leroux, D
Pasquier, B
机构
[1] CHU Grenoble, Hop Albert Michallon, Serv Anat Pathol, Dept Pathol, F-38043 Grenoble 09, France
[2] CHU Grenoble, Dept Pediat, F-38043 Grenoble, France
[3] CHU Grenoble, Lab Cytogenet, F-38043 Grenoble 09, France
[4] Inst Curie, Lab Genet Tumeurs, Paris, France
关键词
desmoplastic small round cell tumor; EWS/WT1 fusion transcript; WT1;
D O I
10.1016/S0344-0338(98)80128-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Desmoplastic small round cell tumor is an aggressive neoplasm first described in 1991. Recently, a reciprocal translocation t(11;22)(p13;q12) has been characterized by conventional cytogenetic studies and molecular analysis. This translocation involves the Ewing's sarcoma gene on chromosome 22 and the Wilms' tumor gene WT1 on chromosome 11. The chimeric transcript corresponding to the fusion gene could be detected by the reverse transcriptase-polymerase chain reaction (RT-PCR). Using an anti-WT1 antibody, the WT1 part of the putative chimeric protein could be recognized by immunohistochemistry. We describe two well-characterized cases of intraabdominal desmoplastic small round cell tumor in two male patients aged 14 and 28 with both RT-PCR analysis and immunostaining for WT1. In this report, we insist on the necessity to increase the RT-PCR analysis in DSRCT in order to obtain a precise differential diagnosis. In addition, WT1 immunostaining may serve as a useful diagnostic marker for DSRCT.
引用
收藏
页码:693 / 700
页数:8
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