British Journal of Anaesthesia, Vol 80, Issue 4 516-518, Copyright © 1998 by The Board of Management and Trustees of the British Journal of Anaesthesia
J. Hernandez-Palazon, J. F. Martinez-Lage, J. A. Tortosa and J. M. Garcia-Cayuela
We report two young patients who had repeated neurosurgical procedures and
who were thought to be at risk of developing Creutzfeldt-Jakob disease
(CJD). The first patient had been given a lyophilized dural graft in the
course of removal of a cerebellar medulloblastoma 15 yr previously. The
second patient had received pituitary-derived growth hormone for treatment
of growth hormone deficiency, secondary to a third ventricle teratoma,
exised 13 yr earlier. The presence of cerebellar symptoms together with
being recipients of growth hormone or dural graft of cadaveric extraction
arose suspicion of a diagnosis of CJD in both individuals. Precautions in
the anaesthetic and surgical management of these two patients are
discussed, and pertinent literature is reviewed briefly.
CASE REPORTS
Anaesthetic management in patients suspected of, or at risk of, having Creutzfeldt-Jakob disease
Department of Anaesthesia, Virgen de la Arrixaca University Hospital, Murcia, Spain; Department of Neurosurgery, Virgen de la Arrixaca University Hospital, Murcia, Spain
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