A congenital medulloepithelioma of the midbrain
A congenital medulloepithelioma of the midbrain
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先天性中脑髓质上皮瘤
DOI:
10.1002/path.1700740214
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发表时间:
1957
期刊:
影响因子:
--
通讯作者:
C. Treip
中科院分区:
文献类型:
--
作者:
C. Treip
IN the histogenetic classification of the gliomas proposed by Bailey and Cushing (1926) the most primitive tumour of the series, postulated as arising from the epithelium of the medullary plate, was described as medulloepithelioma. Bailey and Cushing were able to find only two tumours in their series which they could put under this heading. One arose from the post-infundibular region of the third ventricle, the other from the pineal-sites in which medullary-plate cells, characterised by an internal limiting membrane, persist into post-natal life (Benda, 1898). Both tumours consisted of more or less differentiated tubules of columnar cells, partly stratified and possessing internal and external limiting membranes. One of the tumours showed some formation of perivascular rosettes. In neither did the cells contain cilia or blepharoplasts, though in the second case (p. 54) a diplosome was present in many cells.Since this first description and naming of the tumour very few further examples have been reported (Davie, 1932; Greenfield, 1934) and its existence has been called into question (Mabon et aZ., 1950). The primitive medullary epithelium begins to develop cilia at the end of the fifth week of embryonic life. Russell (1950) has pointed out that cilia persist into adult life and that the ciliated ependymal cell is in fact the mature form; it is the primitive cell that is free of cilia. The very early stage at which cilia develop would explain the extreme rarity with which true medullary epithelium has been found.