Assuntos
Esclerose Múltipla Crônica Progressiva/complicações , Músculo Esquelético/fisiopatologia , Tremor/etiologia , Tremor/fisiopatologia , Adulto , Azatioprina/uso terapêutico , Tronco Encefálico/patologia , Tronco Encefálico/fisiopatologia , Cerebelo/fisiopatologia , Clonazepam/uso terapêutico , Extremidades/inervação , Extremidades/fisiopatologia , Feminino , Moduladores GABAérgicos/uso terapêutico , Humanos , Imunossupressores/uso terapêutico , Esclerose Múltipla Crônica Progressiva/fisiopatologia , Músculo Esquelético/inervação , Vias Neurais/patologia , Vias Neurais/fisiopatologia , Exame NeurológicoRESUMO
Idiopathic ventral spinal cord herniation is a rare cause of progressive myelopathy that demonstrates unique radiological features. We describe a case of thoracic spinal cord herniation through an anterior dural defect and discuss the characteristic findings on magnetic resonance imaging and computed tomographic myelography. A 36-year-old man presented to our clinic with progressive leg weakness and spasticity in both legs. Magnetic resonance imaging of the thoracic spinal canal demonstrated C-shaped anterior kinking of an atrophied spinal cord and enlarged dorsal subarachnoid space at the T5-T6 level. Computed tomographic myelography showed ventral herniation of the spinal cord and no evidence of an intradural spinal arachnoid cyst. Ventral spinal cord herniation is a commonly misdiagnosed entity. Knowledge of the characteristic imaging appearance of this treatable condition is important for proper diagnosis and treatment.
RESUMO
Although nervous system involvement is common in thrombotic thrombocytopenic purpura (TTP), abnormalities on computerized tomography, magnetic resonance imaging and electroencephalography are not encountered so frequently and if present, these abnormalities are often reversible. We describe a 39-year-old woman with recurring transient focal neurological findings found to have laboratory findings consistent with TTP. In cerebral diffusion weighted images (DWI), diffuse cortical hyperintensity was noted in right frontal lobe, but the ADC (apparent diffusion coefficient) map was normal. Electroencephalography demonstrated lateralized slowing and repeated DWI showed diffuse cortical hyperintensity in the right hemisphere. SPECT showed luxury perfusion in the right hemisphere areas. The patient's condition resolved with plasmapheresis. Our patient illustrates that diffuse hemispheric involvement can be seen in DWI and EEG, and SPECT may show luxury perfusion after resolution of neurological findings in TTP cases. To our knowledge, this is the first TTP case in which the ADC map was normal.