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  Vol. 45 No. 7, July 1988 TABLE OF CONTENTS
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Neurocysticercosis

Two Hundred Thirty-Eight Cases From a California Hospital

David Scharf, MD

Arch Neurol. 1988;45(7):777-780.


Abstract



• Neurocysticercosis is no longer a medical curiosity in the United States. Two hundred thirty-eight patients with neurocysticercosis were studied between 1981 and 1986 at the Los Angeles County-University of Southern California Medical Center, Los Angeles. Presenting signs and symptoms were protean—ranging from a single convulsion to coma and death. Fifty-one patients (21%) presented with an acute increase in intracranial pressure. There were 71 patients who ultimately required a shunting procedure or craniotomy. Presentation, diagnosis, management, and laboratory adjuncts (the role of cysticercosis titers and the electroencephalogram) are discussed. Mortality and morbidity can be reduced by maintaining a high degree of suspicion in populations at increased risk for cysticercosis.



Author Affiliations



From the Department of Neurology, Los Angeles County-University of Southern California Medical Center, Los Angeles.


Footnotes



Accepted for publication Dec 21, 1987.

Reprint requests to Department of Neurology, Los Angeles County-University of Southern California Medical Center, Los Angeles, CA 90033 (Dr Scharf).



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