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- W1993766125 abstract "Very great confusion exists as regards terminology of neural tumours and their c1assification. Many apellations and comments have been applied to each of these tumours since the beginning of the century. This confusion is further aggravated by the difficulties of histological diagnosis and by the persistent uncertainty as to the precise origin of these tumours in the nerve tissue. Harkin and Redd (1968) c1assified the tumours into five categories: 1. Neoplasms of nerve sheath origino A. Benign primary nerve sheath tumours. 1. Schwannoma (neurilemmoma). 2. Neurofibroma. B. Malignant primary nerve sheath tumours. 1. Malignant schwannoma. 2. Nerve sheath fibrosarcoma. lI. Neoplasms of nerve cell origino 1. Neuroblastoma. 2. Ganglioneuroma. 3. Pheochromocytoma. lII. Tumours metastatic to peripheral nerves. IV. Neoplasms of non-neural origino 1. Lipofibromatosis. 2. Intraneurallipoma, haemangioma, ganglion. V. Non-neoplasms (traumatic neuroma, compressive neuroma). The neuropathologists c1assify more tumour types into the category of peripheral nerve tumours. Consequently the aboye mentioned list should be completed with the granular cell tumours, with the melanotic neuroectodermal tumours, with the chemodectomas as well as with the tumours of APUD (Amine Precursor Uptake and Decarboxylation) cell origino It seems to be agreed by all present-day authors that three main types of peripheral nerve tumours exist, all arising from the Schwann-cell and secondarily from the fibroblasts of the endoneurium and perineurium: schwannomas (neurilemmomas), neurofibromas and nerve tumours malignant from the outset (neurofibrosarcomas). These are the peripheral nerve tumours with which a neurosurgeon must be familiar." @default.
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- W1993766125 date "1991-01-01" @default.
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- W1993766125 title "Peripheral nerve tumours" @default.
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- W1993766125 doi "https://doi.org/10.1016/s1130-1473(91)71172-x" @default.
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