By Wolfgang Wechsler, Guido Reifenberger (auth.), Masakatsu Nagai M.D., Ph.D. (eds.)
The name of this monograph, mind Tumor examine and remedy, is the identify of the convention itself, which had its inaugural assembly within the usa in 1975 andhas considering improved to the foreign scale. In Japan, the 1st convention ofits style used to be equipped via Dr. Takao Hoshino and me and was once held at Nikko in 1980, therefore its identify, the Nikko convention on mind Tumor examine and remedy. although it began as a small, closed assembly, the convention has grown significantly, and in 1992 it used to be reorganized because the jap convention on mind Tumor examine and remedy and was once opened to all neurosurgeons and neuropathologists drawn to the research of mind tumor difficulties and who're partaking during this box. the most function of the convention on mind Tumor study and treatment is the candid and trained dialogue of the main up to date advancements in easy re seek and medical therapy of mind tumors. The third jap convention on mind Tumor learn and treatment used to be held at Nasu (Tochigi Prefecture), Japan, in No vember 1994. It used to be a good honor to welcome many uncommon site visitors from over seas who kindly attended each one consultation and made useful contributions.
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Histological Aspects of Certain Benign Brain Tumors 23 Pleomorphic Xanthoastrocytoma This rare variant of astrocytoma was described by Kepes et al. in 1979 and reviewed by Kepes in 1993 . It occurs in children or young adults and involves superficial areas of the cerebral hemispheres, especially the temporal lobe. The tumor is often associated with a cyst. As its name implies, this pleomorphic astrocytoma exhibits various froms, ranging from the usual fibrillary astrocytes to giant multinucleated forms.
J Neuropathol Exp Neurol 51:644-657 6. Daumas-Duport C (1993) Dysembryoplastic neuroepithelial tumors. Brain Pathol 3:283295 7. Hirose T, Scheithauer BW, Lopes MBS, VandenBerg SR (1994) Dysembryoplastic neuroepithelial tumor (DNT): an immunohistochemical and ultrastructural study. J Neuropathol Exp Neurol 53:184-195 8. Raymond AA, Halpin SFS, Alsanjari N, Cook MJ, Kitchen ND, Fish DR, Steven JM, Harding BN, Scaravilli F, Kendall B, Shorvon SD, Neville BGR (1994) Dysembryoplastic neuroepithelial tumor.
The first case was an ll-year-old boy with a family history of tuberous sclerosis. Although there was no neurological symptom, bilateral papilledema was found on routine ophthalmological examination and a large circumscribed intraventricular mass was identified by computed tomography (CT). The second case was a 4-year-old boy with no family history of tuberous sclerosis. This patient underwent partial resection of a large tumor in the region of the foramen of Monro in May 1990 and then total tumor removal in October 1990.
Brain Tumor: Research and Therapy by Wolfgang Wechsler, Guido Reifenberger (auth.), Masakatsu Nagai M.D., Ph.D. (eds.)