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Perfusion Imaging in Autoimmune Encephalitis. | LitMetric

AI Article Synopsis

  • Encephalitis involves inflammation of the brain and can have infectious and noninfectious origins, with specific diagnostic tools like CSF analysis and MRI typically showing inflammatory changes.
  • A case study presented a 65-year-old woman with a fall and confusion, where initial tests for infections were negative, but brain imaging showed abnormal findings, complicating the diagnosis.
  • Ultimately, after treatment failures, she tested positive for GAD65 antibodies, indicating autoimmune encephalitis, and her symptoms drastically improved with plasmapheresis, marking a unique case due to its unusual imaging characteristics.

Article Abstract

Encephalitis is characterized by inflammation of brain tissue and has various infectious and noninfectious causes. CSF analysis and MRI usually reveal inflammatory changes although sometimes brain imaging may be normal. Autoimmune encephalitis is caused by antibodies against neuronal synaptic receptors, surface proteins, or intracellular proteins. In this case report, we present a 65-year-old female who presented with a fall and altered mental status. Workup for infectious etiologies was negative and MRI of the brain displayed focal restricted diffusion with corresponding T2-FLAIR hyperintensity involving gray matter structures, making the diagnosis unclear. CT perfusion of the brain demonstrated increased cerebral blood volume and cerebral blood flow in the left parietooccipital gray matter, with corresponding normal mean transit time. Following treatment failure with acyclovir, antibiotics, and steroids, the patient was found to be positive for GAD65 antibodies and diagnosed with autoimmune encephalitis. Symptoms markedly improved with plasmapheresis. Autoimmune encephalitis rarely causes restricted diffusion and this is the first case report to describe corresponding hyperperfusion on CT perfusion study.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960559PMC
http://dx.doi.org/10.1155/2018/3538645DOI Listing

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