Gliosarcoma

Pathology, Neurology, Ophthalmology

Also known as: Glioma Sarcomatodes, Glioplastic Sarcoma

Historical document, translated for reference. It reflects medical knowledge of the 1920s–30s and is not medical advice.

Summary

Gliosarcoma is considered by most authors to be a variety of glioma, specifically a soft glioma rich in neuroglial cells and containing few differentiated neuroglial fibers. Some propose to retain the term gliosarcoma only for cases where there is combined growth of ectodermal and mesodermal elements (glioma + sarcoma).

Encyclopedia entry (1928–1936)

GLIOSARCOMA, or (according to Borst) glioma sarcomatodes, glioplastic sarcoma, represents, in the opinion of most authors, a variety of glioma (see), specifically a soft glioma rich in neuroglial cells and containing almost no differentiated neuroglial fibers. Some propose to retain the term G. only for those cases where there is combined growth of ectodermal and mesodermal elements (glioma + sarcoma). Typical (purely neuroglial) gliosarcomas microscopically resemble round-cell sarcoma; clinically, however, they are less malignant, usually do not metastasize; sometimes infiltration of the meninges, bones, and soft tissues by the tumor is observed. The most frequent location of G. is the retina (see). Lit.—see lit. to article Glioma.

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Cite this page

“Gliosarcoma.” Soviet Medical Encyclopedia. English translation of Bolshaya Meditsinskaya Entsiklopediya, 1st ed. (Moscow, 1928–1936), ed. N. A. Semashko. https://sovietmedicalencyclopedia.pages.dev/article/gliosarcoma/