Neurocisticercosis racemosa subaracnoidea gigante y ventricular: a propósito de un caso
Author(s) -
Álvaro SánchezLarsen,
María Elena Artiles Monteagudo,
E. Lozano-Setién,
Jorge GarcíaGarcía
Publication year - 2015
Publication title -
revista argentina de microbiología
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 26
eISSN - 1851-7617
pISSN - 0325-7541
DOI - 10.1016/j.ram.2015.07.001
Subject(s) - neurocysticercosis , albendazole , medicine , taenia solium , context (archaeology) , praziquantel , parasitic disease , serology , disease , cysticercosis , surgery , pediatrics , pathology , immunology , biology , helminths , schistosomiasis , paleontology , antibody
Neurocysticercosis is the most frequent parasitic disease of the central nervous system. It is caused by the larvae of Taenia solium, which can affect different anatomical sites. In Spain there is an increasing prevalence mainly due to immigration from endemic areas. The extraparenchymal forms are less common, but more serious because they usually develop complications. Neuroimaging plays a major role in the diagnosis and follow-up of this disease, supported by serology and a compatible clinical and epidemiological context. First-line treatments are cysticidal drugs such as albendazole and praziquantel, usually coadministered with corticosteroids, and in some cases surgery is indicated. We here report a case of neurocysticercosis with simultaneous intraventricular and giant racemose subarachnoid involvement.
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