| Literature DB >> 21716628 |
Jong Hun Seo1, Hong Ju Seo, Seok Won Kim, Ho Shin.
Abstract
Spinal intradural cysticercosis is a rare manifestation of neurocysticercosis. We report a unique patient who showed visual symptoms and normal imaging of the brain caused by isolated spinal neurocysticercosis. A 59-year-old male patient was admitted to the emergency unit with a history of severe headache and progressive blurred vision. Brain computed tomographic scanning and magnetic resonance imaging showed normal cerebral anatomy without hydrocephalus. The fundoscopic evaluation by an ophthalmologist showed bilateral papilledema. Perimetry studies revealed visual field defects in both eyes. With the diagnosis of pseudotumor cerebri, a lumbar tap was attempted; however, we could not drain the cerebrospinal fluid in spite of appropriate attempts. Lumbar magnetic resonance imaging revealed multilevel intraspinal lesions that were confirmed histologically to be neurocysticercosis. An intraoperative lumbar puncture revealed an increased opening pressure and cytochemical analysis showed elevated cerebrospinal fluid protein level. The headache resolved immediately after surgery. However, the visual symptoms remained and recovered only marginally despite antihelminthic medications after six months of operation.Entities:
Keywords: Cerebrospinal spinal fluid; Pseudotumor cerebri; Spinal neurocysticercosis
Year: 2011 PMID: 21716628 PMCID: PMC3115153 DOI: 10.3340/jkns.2011.49.5.296
Source DB: PubMed Journal: J Korean Neurosurg Soc ISSN: 1225-8245