Immunohistochemistry of primary central nervous system malignant rhabdoid tumors: Report of five cases and review of the literature

被引:33
作者
Behring, B
Bruck, W
Goebel, HH
Behnke, J
Pekrun, A
Christen, HJ
Kretzschmar, HA
机构
[1] UNIV GOTTINGEN, INST NEUROPATHOL, D-37075 GOTTINGEN, GERMANY
[2] UNIV MAINZ, DEPT NEUROPATHOL, MAINZ, GERMANY
[3] UNIV GOTTINGEN, DEPT NEUROSURG, W-3400 GOTTINGEN, GERMANY
[4] UNIV GOTTINGEN, DEPT PEDIAT, W-3400 GOTTINGEN, GERMANY
[5] UNIV GOTTINGEN, DEPT NEUROPEDIAT, W-3400 GOTTINGEN, GERMANY
关键词
malignant rhabdoid tumor; immunohistochemistry; central nervous system;
D O I
10.1007/s004010050470
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Malignant rhabdoid tumors (MRT) are characterized by a typical light microscopic morphology with uniformly round tumor cells, vacuolated cytoplasm with occasional round, hyaline intracytoplasmic, periodic acid-Schiff-positive inclusions, vesicular nuclei with prominent nucleoli and positive immunoreactivity for vimentin. The histogenesis of MRT is controversial. Five cases of primary central nervous system (CNS) rhabdoid tumors in children are presented. Immunohistochemical, light and electron microscopic features are compared with primary CNS malignant rhabdoid tumors reported in the literature. Expression of various neurofilaments in our cases of primary CNS rhabdoid tumors was prominent and we therefore favor a neural differentiation of extrarenal intracerebral rhabdoid tumors.
引用
收藏
页码:578 / 586
页数:9
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