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- W2037808154 abstract "The clinical picture of primary diffuse meningiomatosis comprises: 1.(1) A meningeal syndrome with cyto-albuminous dissociation and raised pressure in the cerebrospinal fluid. 2.(2) A spinal polyradicular syndrome, anterior or posterior, or a cranial polyneuritis. This root syndrome can present itself in the form of a posterior radicular syndrome with pain and loss of reflexes; or as a cauda equina lesion with sphincter disturbances, sensory loss and motor defect; or yet again as a picture of multiple cranial nerve palsies especially involving the optic and the oculomotor nerves and later all the other nerves. It is the association of meningeal and radicular signs which is characteristic. The absence of signs indicating involvement of the parenchyma like the lack of a Brown-Séquard syndrome or of a syringomyelic dissociation, completes the initial picture. At first, the grouping of clinical signs produces a division into two types: a cerebro-cerebellar form, and a spinal type. The course is a progressive one. Gradually fresh signs appear and the cerebral type becomes generalized through the involvement of spinal segments, while the spinal type later involves the posterior forsa and the basal cisterns. In the terminal stages the patient now being cachectic, the whole symptomatology is to be found." @default.
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- W2037808154 title "Le syndrome anatomo-clinique des méningiomatoses" @default.
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- W2037808154 doi "https://doi.org/10.1016/0022-510x(65)90063-8" @default.
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