Ciencias,UNAM

Proposed diagnostic criteria for neurocysticercosis

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dc.contributor.author Del Brutto, OH
dc.contributor.author Rajshekhar, V
dc.contributor.author White, AC
dc.contributor.author Tsang, VCW
dc.contributor.author Nash, TE
dc.contributor.author Takayanagui, OM
dc.contributor.author Schantz, PM
dc.contributor.author Evans, CAW
dc.contributor.author Flisser, A
dc.contributor.author Correa, D
dc.contributor.author Botero, D
dc.contributor.author Allan, JC
dc.contributor.author Sarti, E
dc.contributor.author González, AE
dc.contributor.author Gilman, RH
dc.contributor.author García, HH
dc.date.accessioned 2011-12-07T13:39:23Z
dc.date.accessioned 2014-01-28T15:17:03Z
dc.date.available 2011-12-07T13:39:23Z
dc.date.available 2014-01-28T15:17:03Z
dc.date.issued 2001
dc.identifier.citation Del Brutto, OH; Rajshekhar, V; White, AC; Tsang, VCW; Nash, TE; Takayanagui, OM; Schantz, PM; Evans, CAW; Flisser, A; Correa, D; Botero, D; Allan, JC; Sarti, E; González, AE; Gilman, RH; García, HH. (2001). Proposed diagnostic criteria for neurocysticercosis. Neurology, 57(2), 177-183.
dc.identifier.issn 0028-3878
dc.identifier.uri http://hdl.handle.net/11154/99985
dc.identifier.uri http://hdl.handle.net/11154/174523
dc.description.abstract Neurocysticercosis is the most common helminthic infection of the CNS but its diagnosis remains difficult. Clinical manifestations are nonspecific, most neuroimaging findings are not pathognomonic, and some serologic tests have low sensitivity and specificity. The authors provide diagnostic criteria for neurocysticercosis based on objective clinical, imaging, immunologic, and epidemiologic data. These include four categories of criteria stratified on the basis of their diagnostic strength, including the following: 1) absolute-histologic demonstration of the parasite from biopsy of a brain or spinal cord lesion, cystic lesions showing the scolex on CT or MRI, and direct visualization of subretinal parasites by funduscopic examination; 2) major-lesions highly suggestive of neurocysticercosis on neuroimaging studies, positive serum enzyme-linked immunoelectrotransfer blot for the detection of anticysticercal antibodies, resolution of intracranial cystic lesions after therapy with albendazole or praziquantel, and spontaneous resolution of small single enhancing lesions; 3) minor-lesions compatible with neurocysticercosis on neuroimaging studies, clinical manifestations suggestive of neurocysticercosis, positive CSF enzyme-linked immunosorbent assay for detection of anticysticercal antibodies or cysticercal antigens, and cysticercosis outside the CNS; and 4) epidemiologic-evidence of a household contact with Taenia solium infection, individuals coming from or living in an area where cysticercosis is endemic, and history of frequent travel to disease-endemic areas. Interpretation of these criteria permits two degrees of diagnostic certainty: 1) definitive diagnosis, in patients who have one absolute criterion or in those who have two major plus one minor and one epidemiologic criterion; and 2) probable diagnosis, in patients who have one major plus two minor criteria, in those who have one major plus one minor and one epidemiologic criterion, and in those who have three minor plus one epidemiologic criterion.
dc.language.iso en
dc.publisher Neurology
dc.subject.classification 771
dc.title Proposed diagnostic criteria for neurocysticercosis
dc.type Article
dc.relation.index WoS

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