Download Craniopharyngioma: Surgical Treatment by A. Allegranza (auth.), Giovanni Broggi M.D. (eds.) PDF

By A. Allegranza (auth.), Giovanni Broggi M.D. (eds.)
Craniopharyngioma represents an enormous problem for neurosurgeons, pediatricians, and endocrinologists. This so-called benign tumor is a true possibility to caliber of lifestyles and lifestyles itself. This ebook discusses a number of the healing concepts and indicates multimodal remedy techniques, together with microsurgery, stereotaxis, and substitute remedies. the explanation for collection of remedy is supported through organic, scientific, and neuroradiological facts and healing result of a wide sequence of case reviews from around the world are stated. ultimately, directions for extra improvement and new issues for examine and therapy are offered.
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Extra resources for Craniopharyngioma: Surgical Treatment
Example text
1990). Intrasellar tumor or those with only a small suprasellar component clearly are best operated using the trans sphenoidal approach (Laws 1980). Approach through the temporal fossa has been advocated for those tumors which have a sizable retrosellar component (Symon and Sprich 1985). Finally, a bifrontal approach can be useful, enabling the surgeon to work laterally to both of the optic nerves and tracts (Sarnii and Bini 1991). The author believes that each of these approaches is useful and may be employed when the occasion demands.
This higher percentage reflects that in a number of these patients the operator felt that the tumor was totally removed, only to be shown to be wrong on postoperative CT or magnetic resonance imaging (MRl) scanning. These "inadvertent" tumor remnants were removed with greater facility. Radical Removal of Craniopharyngiomas 1971-1991 35 Secondary Operations The following two cases illustrate that reoperation after initial operative intervention, radiation therapy (including high intensity radiation therapy), or both does not preclude total tumor removal.
The duration of preoperative symptoms is an important prognostic factor. In cases of severe preoperative visual deficit we recommend decompressing the optic pathways in a first stage before dissecting the tumor and removing it. It is clear that total removal of the lesion gives the best ophthalmological results. 28 M. Choux et al. 2) Neurological Results Postoperative neurological deficits are rare. 7% (Shapiro et al. 4% (Pierre-Kahn et al. 1988). In our cooperative series late epilepsy is described in 16% of the cases.