Double immunolabeling of central nervous system atypical teratold/rhabdoid tumors

被引:10
作者
Bouffard, JP
Sandberg, GD
Golden, JA
Rorke, LB
机构
[1] Armed Forces Inst Pathol, Dept Neuropathol & Ophthalm Pathol, Washington, DC 20206 USA
[2] Childrens Hosp Philadelphia, Dept Pathol, Philadelphia, PA 19104 USA
关键词
rhabdoid; central nervous system; primitive neuroectodermal tumor;
D O I
10.1038/modpathol.3800099
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The central nervous system atypical teratoid/rhabdoid tumor (ATRT) is a highly malignant tumor with a heterogeneous immumohistochemical profile and with some morphologic similarity to central nervous system primitive neuroectodermal tumors (PNET). Although several studies have investigated double immunolabeling in PNET, we are aware of no studies of double labeling of ATRT. A total of 10 ATRT from surgical and consultation materials at the Children's Hospital of Philadelphia were selected and stained for a variety of antigens using indirect immunofluorescence to detect single and double labeling. Most tumor cells showed only single labeling; rare cells showed double labeling as follows: 70% of tumors coexpressed (VIM) and glial flibrillary acidic protein (GFAP), 30% smooth muscle actin and GFAP, 20% epithellial membrane antigen (EMA) and VIM, 20% EMA/GFAP, and 20% EMA/SMA. These results are discussed in view of current debates over the histogenesis of CNS PNET and ATRT, and in reference to the classification of rhabdoid tumors as an entity or phenotype.
引用
收藏
页码:679 / 683
页数:5
相关论文
共 23 条
[1]   WILMS TUMOR AND OTHER RENAL TUMORS OF CHILDHOOD - A SELECTIVE REVIEW FROM THE NATIONAL-WILMS-TUMOR-STUDY-PATHOLOGY-CENTER [J].
BECKWITH, JB .
HUMAN PATHOLOGY, 1983, 14 (06) :481-492
[2]  
BECKWITH JB, 1978, CANCER-AM CANCER SOC, V41, P1937, DOI 10.1002/1097-0142(197805)41:5<1937::AID-CNCR2820410538>3.0.CO
[3]  
2-U
[4]   ESTABLISHMENT AND CHARACTERIZATION OF THE HUMAN MEDULLOBLASTOMA CELL-LINE AND TRANSPLANTABLE XENOGRAFT D283-MED [J].
FRIEDMAN, HS ;
BURGER, PC ;
BIGNER, SH ;
TROJANOWSKI, JQ ;
WIKSTRAND, CJ ;
HALPERIN, EC ;
BIGNER, DD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1985, 44 (06) :592-605
[5]  
FRIEDMAN HS, 1988, AM J PATHOL, V130, P472
[6]   Chromosome 22q dosage in composite extrarenal rhabdoid tumors: Clonal evolution or a phenotypic mimic? [J].
Fuller, CE ;
Pfeifer, J ;
Humphrey, P ;
Bruch, LA ;
Dehner, LP ;
Perry, A .
HUMAN PATHOLOGY, 2001, 32 (10) :1102-1108
[7]   Collision of uterine rhabdoid tumor and endometrioid adenocarcinoma: A case report and review of the literature [J].
Gaertner, EM ;
Farley, JH ;
Taylor, RR ;
Silver, SA .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1999, 18 (04) :396-401
[8]  
GOULD VE, 1990, LAB INVEST, V62, P498
[9]   PRIMITIVE NEUROECTODERMAL TUMORS OF THE CENTRAL-NERVOUS-SYSTEM EXPRESS NEUROENDOCRINE MARKERS AND MAY EXPRESS ALL CLASSES OF INTERMEDIATE FILAMENTS [J].
GOULD, VE ;
RORKE, LB ;
JANSSON, DS ;
MOLENAAR, WM ;
TROJANOWSKI, JQ ;
LEE, VMY ;
PACKER, RJ ;
FRANKE, WW .
HUMAN PATHOLOGY, 1990, 21 (03) :245-252
[10]   PHENOTYPIC ANALYSIS OF 4 HUMAN MEDULLOBLASTOMA CELL-LINES AND TRANSPLANTABLE XENOGRAFTS [J].
HE, XM ;
SKAPEK, SX ;
WIKSTRAND, CJ ;
FRIEDMAN, HS ;
TROJANOWSKI, JQ ;
KEMSHEAD, JT ;
COAKHAM, HB ;
BIGNER, SH ;
BIGNER, DD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1989, 48 (01) :48-68