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Medullomyoblastoma in an adult.

Authors :
Rao C
Friedlander ME
Klein E
Anzil AP
Sher JH
Source :
Cancer [Cancer] 1990 Jan 01; Vol. 65 (1), pp. 157-63.
Publication Year :
1990

Abstract

Medullomyoblastoma is a rare histologic variant of medulloblastoma. Of the 20 cases reported in the literature, 19 were in children ages 2.5 to 10.5 years and one was in a 26-year-old woman. In the reported adult case the myogenic component of the tumor was leiomyosarcomatous. The authors report a case of medullomyoblastoma with a rhabdomyosarcomatous component in a 40-year-old man with light microscopic, immunohistochemical, and ultrastructural findings. The histogenetic theories regarding this tumor include that it is a teratoma, or that the myogenic component arises from the perivascular or leptomeningeal ectomesenchyme, or pluripotential neuroectodermal cells, or endothelial cells. The authors' findings do not elucidate the histogenesis but argue against an endothelial origin of the rhabdomyoblastic component.

Details

Language :
English
ISSN :
0008-543X
Volume :
65
Issue :
1
Database :
MEDLINE
Journal :
Cancer
Publication Type :
Academic Journal
Accession number :
2403482
Full Text :
https://doi.org/10.1002/1097-0142(19900101)65:1<157::aid-cncr2820650130>3.0.co;2-m