ABSTRACT
Human toxocariasis is a zoonotic parasitic disease caused by Toxocara canis or Toxocara cati larvae. Human infection is usually an outcome of accidental ingestion of the embryonated eggs, and the involvement of central nervous system is rare. We report a case of cerebral infarction which was caused by toxocariasis in adult, who had headache, abdominal pain and right side weakness. He had only a history of ingestion of raw liver of deer.
Subject(s)
Adult , Humans , Abdominal Pain , Central Nervous System , Cerebral Infarction , Deer , Eating , Eggs , Headache , Larva , Liver , Ovum , Parasitic Diseases , Toxocara , Toxocara canis , ToxocariasisABSTRACT
BACKGROUND AND OBJECTIVES: Herpes zoster(HZ) is a well known viral infection of the nervous system. HZ is associated with the neurologic complication. It may have been expected a change in the cerebrospinal fluid(CSF) of patients with HZ. The purpose of this paper is to present the correlation between CSF findings and neurologic complications in HZ. METHOD: The patients(n=75) with HZ were 31 male and 26 females, who were ranged in age from 15 to 79years(mean 53.4 years) admitted to department of Neurology of Chung Ang Gil General Hospital from June 1992 to May 1995. The patients were evaluated for the etiology, lesion distribution, and complications. CSF study was performed in 32 patients(male/female=20/12), whose age ranged from 16 to 79 years(means 51years) during 5 days to 10days after initial symptom onset. CSF findings were analyzed for their etiology, lesion distribution and complication. RESULTS: The CSF of 25 patients(78.1%) showed pleocytosis(5 to 49/mm3 in 10 patients, means, 62.1/mm3). 7 patients(12.3%) had meningitis symptoms, whose cell counts of CSF were more than 50/mm3(means 128.4/mm3) postherapeutic neuralgia was more common in elder patient than younger patients(p=0.005). Complications tended to correlate with the cell counts of CSF. There was no difference in CSF finding between cranial segmental involvements. CONCLUSION: We confirmed the pleocytosis in CSF of patients with HZ and suggest the development of complications in patients in patients with HZ tend to correlate with the cell counts of CSF.
Subject(s)
Female , Humans , Male , Cell Count , Herpes Zoster , Hospitals, General , Leukocytosis , Meningitis , Nervous System , Neuralgia , NeurologyABSTRACT
BACKGROUND AND OBJECTIVES: Herpes zoster(HZ) is a well known viral infection of the nervous system. HZ is associated with the neurologic complication. It may have been expected a change in the cerebrospinal fluid(CSF) of patients with HZ. The purpose of this paper is to present the correlation between CSF findings and neurologic complications in HZ. METHOD: The patients(n=75) with HZ were 31 male and 26 females, who were ranged in age from 15 to 79years(mean 53.4 years) admitted to department of Neurology of Chung Ang Gil General Hospital from June 1992 to May 1995. The patients were evaluated for the etiology, lesion distribution, and complications. CSF study was performed in 32 patients(male/female=20/12), whose age ranged from 16 to 79 years(means 51years) during 5 days to 10days after initial symptom onset. CSF findings were analyzed for their etiology, lesion distribution and complication. RESULTS: The CSF of 25 patients(78.1%) showed pleocytosis(5 to 49/mm3 in 10 patients, means, 62.1/mm3). 7 patients(12.3%) had meningitis symptoms, whose cell counts of CSF were more than 50/mm3(means 128.4/mm3) postherapeutic neuralgia was more common in elder patient than younger patients(p=0.005). Complications tended to correlate with the cell counts of CSF. There was no difference in CSF finding between cranial segmental involvements. CONCLUSION: We confirmed the pleocytosis in CSF of patients with HZ and suggest the development of complications in patients in patients with HZ tend to correlate with the cell counts of CSF.
Subject(s)
Female , Humans , Male , Cell Count , Herpes Zoster , Hospitals, General , Leukocytosis , Meningitis , Nervous System , Neuralgia , NeurologyABSTRACT
Ophthalmoplegic migraine is a syndrome characterized by the typical history of migrainous headache followed by ophthalmoplegia in the absence of demonstrable intracranial lesion. Until now, investigations of regional cerebral blood flow (CBF) in patient,; with migraine have been performed during prodromal and/or headache phases by brain SPECT with Tc-99m HMPAO. However, no such paper has described patients with ophthalmoplegic migraine. We present a 14-year-old girl with 4 episodes of paroxysmal migrainous headache on the right fronto-orbital area without aura followed by ptosis and diplopia, which were always gradually resolved without aberrant regeneration over 2 or 3 weeks period. Neurologic examination showed the right internal and external ophthalmoplegia. Diagnostic studies (including laboratory testis, Tensilon test, brain MRI, and cerebral angiography) were normal. Serial brain SPECT studies with Tc-99m HMPAO showed the presence of reversible ischemia in the branches of the posterior cerebral artery.
Subject(s)
Adolescent , Female , Humans , Brain , Diplopia , Edrophonium , Epilepsy , Headache , Ischemia , Magnetic Resonance Imaging , Migraine Disorders , Neurologic Examination , Ophthalmoplegia , Ophthalmoplegic Migraine , Posterior Cerebral Artery , Regeneration , Technetium Tc 99m Exametazime , Testis , Tomography, Emission-Computed, Single-PhotonABSTRACT
A child, aged 4-year-old girl was admitted to our hospital because of impaired vision and right hemiparesis. Brain MRI showed a lesion in the left parietal white matter, and visual evoked potentials and brainstem evoked potentials gave abnormal findings showing lesions also of the optic nerves and brainstem. Her symptoms were resolved with steroid therapy. Afterwards, she had 3 episodes of spastic paraparesis, cerebellar syndrome, downbeat nystagmus, and clinical seizures for a year. With a history of remissions and exacerbations and brain MRls that revealed new scattered lesions each time, the diagnosis of multiple sclerosis was able to be made. This is the one of the youngest of known patients with MS, yet described, in Korea, whose first attack occurred at 4 years old of age.
Subject(s)
Child , Child, Preschool , Female , Humans , Brain , Brain Stem , Cerebellar Diseases , Diagnosis , Evoked Potentials , Evoked Potentials, Visual , Korea , Magnetic Resonance Imaging , Multiple Sclerosis , Optic Nerve , Paraparesis, Spastic , Paresis , Rabeprazole , SeizuresABSTRACT
Fibromuscular dysplasia (FMD) is a segmental nonatheromatous and noninflammatory angiopathy of unknown cause. Despite the unknown origin Of FMD, it has been recognized in the extracranial internal cartid, vertebral, and intracranial arteries. Usually the diagonsis of FMD has been done by angiographic findings, and pathologically proven cases are very rare. We report 2 patients who had suffered from hemicranial pain and ipsilateral ama-urosis figax, and whose initial laboratory evaluations revealed high ESR. The biopsy was done in the temporal artery under the impression of the temporal arteritis, which showed the findings of the fibromuscular dysplasia.