AMAarchives of neurology & psychiatry . Fig. 4. — Ganglion cell in the center packed with granules (fuchsinophil,lichtgriin and other catabolic products). The rest are swollen and greatly lique-fied ganglions. Lichtgriin-fuchsin: Alzheimer method VI; X The included cancer cells stained much more brilliantly than did theganglion cells, and thus gave the section a deeply colored places the greatly swollen ganglion cells were pressed so closelytogether as to form giant cells containing several nuclei. It was notalways easy to differentiate between the nuclei of the host and th


AMAarchives of neurology & psychiatry . Fig. 4. — Ganglion cell in the center packed with granules (fuchsinophil,lichtgriin and other catabolic products). The rest are swollen and greatly lique-fied ganglions. Lichtgriin-fuchsin: Alzheimer method VI; X The included cancer cells stained much more brilliantly than did theganglion cells, and thus gave the section a deeply colored places the greatly swollen ganglion cells were pressed so closelytogether as to form giant cells containing several nuclei. It was notalways easy to differentiate between the nuclei of the host and thoseof the included cancer cells. Some of the most damaged ganglion cells appeared structureless,colorless, devoid of chromatin and often without inclusions (Fig. 4) HASSIX-SIXGER—CEREBRAL CARCIXOMA 161 but with a large pale nucleus, free from chromatin but possessing amembrane and visible nucleolus. Many could be recognized only by acareful study of the numerous transition types. So manifold werethese that description is impossible. Some conception of the ;ize and general appearance may be gained from Figs. 3. 4 and 5. The]jrocess in general appeared to be progressive liquefaction and tumefac-tion with neuronophagy, the invaders being canc


Size: 1484px × 1684px
Photo credit: © The Reading Room / Alamy / Afripics
License: Licensed
Model Released: No

Keywords: ., bookcentury1900, bookdecade1910, bookpublisherchica, bookyear1919