30 June 2008
Intradural-extramedullary spinal cysticercosis without parenchymal involvement
Charles M. Edwards, Ana Miranda, Stephanie PezzoAm J Case Rep 2008; 9:301-303 :: ID: 863371
Abstract
Background: Neurocysticercosis is being encountered with increasing frequency in non-endemic areas. The disease has a broad variety of clinical and radiographic presentations that can make the diagnosis a challenge for clinicians.
Case Report: A 31-year-old male presented with chronic headaches and blurry vision. A computed-tomography scan of the head showed marked hydrocephalous and cerebral spinal fluid (CSF) analysis revealed a mild pleocytosis with eosinophilia. Subsequent magnetic resonance imaging (MRI) demonstrated an isolated intradural-extramedullary cyst in the cervical region without evidence of intraparenchymal involvement. CSF serology confirmed the diagnosis of neurocysticercosis. This represented an extremely rare presentation of neurocysticercosis that has few reports in the literature.
Conclusions: Neurocysticercosis should be included in the differential diagnosis of any patient found to have eosinophilic meningitis or who presents with unexplained seizures. A thorough understanding of the variable radiographic presentations of neurocysticercosis is required in order to effectively diagnose
this increasingly common disease.
Keywords: neurocysticersosis, eosinophilic meningitis, hydrocephalous
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.953173
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.953192
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.952818
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.953608
Most Viewed Current Articles
07 Dec 2021 : Case report
22,364,578
DOI :10.12659/AJCR.934347
Am J Case Rep 2021; 22:e934347
06 Dec 2021 : Case report
174,245
DOI :10.12659/AJCR.934406
Am J Case Rep 2021; 22:e934406
21 Jun 2024 : Case report
119,744
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
64,648
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133






