Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 48 (1979), S. 177-190 
    ISSN: 0942-0940
    Keywords: Optic nerve glioma ; tissue culture ; piloid astrocytes ; immature glia cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cytological characteristics of optic nerve gliomas were studied parallel with histological structures in cell and tissue cultures. Histologically the tumours consisted of four different cell types: spindle-shaped elongated cells, round cells, stellate forms, and multinucleated cells. Dynamic properties of cultured optic glioma cells showed that stable cellular elements of the parent tissue arise from two fundamental populations, viz from elongated (piloid), and from round cells. Cells of both populations displayed a series of changes in the course of their culture. A certain part of the slender elongated cells enlarged and became plump piloid cells of various shapes, or big stellate astrocytes. Giant multinucleated variants of these forms also emerged by fusion of the mononucleate forms. The round cells gradually turned into immature Astrocytes, and by a subsequent cell fusion they gave birth to big stellate cells. With the ageing of the cultures a polymorphous cellular picture developed which was mainly due to the active migratory and intracellular movements of the elongated and round cellular elements. Mitoses played a negligible role in this process. Several characteristics suggest that the round shapes are immature glia cells, and represent the least differentiated elements among all the cell components. The stellate and giant multinucleated forms might be considered as end-products of glia cell differentiation and they could originate both from the elongated and the round cells.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 44 (1978), S. 135-139 
    ISSN: 1432-0533
    Keywords: Tissue culture ; Recurrences of astrocytomas ; Recurrences of oligodendrogliomas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We report a tissue culture study of 50 recurrent supratentorial gliomas. From the initial and recurrent operations 23 astrocytomas and 8 oligodendrogliomas were cultured. 15 astrocytomas and 4 oligodendrogliomas were explanted at the time of recurrence only. On the basis of a three-stage grading system 6 astrocytomas were originally classified as A 1, and 17 as A 2 on cultivation. Oligodendrogliomas proved originally to be O 1 in three cases, and O 2 in five cases. After reoperations all of the A 1 astrocytomas became A 2, 16 A 2 astrocytomas remained unchanged, one A 2 astrocytoma changed, to a glioblastoma. After the third operation one A 2 astrocytoma retained its character, and another one transformed to a glioblastoma. All recurrences of O 1 oligodendrogliomas changed to O 2, and one of them retained this character after the third and fourth operations as well. In the O 2 group, two recurrent oligodendroglioma were unchanged, and three became glioblastomas. The second recurrence of a single O 2 oligodendroglioma showed transformation to a glioblastoma. Cultures indicated a high tendency toward malignant changes, both in astrocytomas and oligodendrogliomas. These changes were closely connected with the presence of immature glial cells. By comparing the tissue culture findings with the clinical data, we conclude that on the basis of cytological malignancy an exact prediction of clinical recurrence is not possible.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...