Titlebook: MRI Atlas of Central Nervous System Tumors; Lucia Cecconi,Alfredo Pompili,Ettore Squillaci Book 1992 Springer-Verlag/Wien 1992 Nervous Sys

Mendacious

myopia

JOG

Commonplace

Meningiomas,e from the outer sheet of the arachnoid. According to their staminal mesodermal cell, they may differentiate as fibroblastic, chondroblastic, etc. They vary in histologic type depending on the amount of fibroblasts (transitional and fibroblastic m.), of calcium deposits (psammomatous m.), and on the

artifice

Pituitary adenomas and craniopharyngiomas,f the hormone that they release and of the clinical syndrome that they induce: prolactin (PRL)-secreting, growth hormone (GH)-secreting, adrenocorticotropin (ACTH)-secreting, which give rise to amenorrhea-galactorrhea, acromegaly and to Cushings’s syndrome, respectively. Very rare pituitary tumors p

Musculoskeletal

Intracranial metastatic tumors, in the tissue. They are believed to prefer the more richly vascularized districts (boundary between the cortex and the white matter), but this assumption is not unanimous, just as there are discordant views on their predilection for the left hemisphere.

Interferons

Rare tumors and nontumoral space-occupying lesions, deal with mass-effect lesions due to malformations, parasitic and infectious diseases which have a tumor-like clinical behavior, together with some cases of lesions of the cranial vault. Given the differences among such lesions, their coverage in this chapter may appear as just another list of dise

增長(zhǎng)

責(zé)怪

Living-Will