Neurocysticercosis
- 1 July 1988
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 45 (7) , 777-780
- https://doi.org/10.1001/archneur.1988.00520310087022
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.This publication has 16 references indexed in Scilit:
- Cerebral cysticercosisQJM: An International Journal of Medicine, 2018
- Cysticercosis of the Human Nervous SystemPublished by Springer Nature ,2014
- Case 11-1986: CysticercosisNew England Journal of Medicine, 1987
- ELISA in the Diagnosis of NeurocysticercosisArchives of Neurology, 1986
- Cysticercosis: A Modern Day PlaguePediatric Clinics of North America, 1985
- Cysticercosis and TaeniasisNew England Journal of Medicine, 1985
- Neurocysticercosis: a new classification based on active and inactive forms. A study of 753 casesArchives of internal medicine (1960), 1985
- Recent Advances in the Diagnosis and Treatment of Cerebral CysticercosisNew England Journal of Medicine, 1984
- CNS CysticercosisArchives of Neurology, 1982
- Cysticercosis Cerebri Review of 127 CasesArchives of Neurology, 1982