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Autoimmune encephalitis (AIE) is a type of encephalitis, and one of the most common causes of noninfectious encephalitis. It can be triggered by tumors , infections , or it may be cryptogenic . The neurological manifestations can be either acute or subacute and usually develop within six weeks.
MRI: Exclusion of differential diagnosis (e.g. cerebrovascular disease). Hyperintensity of affected regions on T2-images is characteristic. Sensitivity 60-84 %. [4] [6] EEG: Exclusion of differential diagnosis. Non-characteristic findings may be found in autoimmune encephalitis. Lumbar puncture: Exclusion of differential diagnosis (e.g ...
Limbic encephalitis is associated with an autoimmune reaction. [1] In non-paraneoplastic limbic encephalitis, this is typically due to infection (commonly herpes simplex virus) or as a systemic autoimmune disorder. [13] Limbic encephalitis associated with cancer or tumors is called paraneoplastic limbic encephalitis. [citation needed]
Encephalitis with meningitis is known as meningoencephalitis, while encephalitis with involvement of the spinal cord is known as encephalomyelitis. [ 2 ] The word is from Ancient Greek ἐγκέφαλος , enképhalos 'brain', [ 37 ] composed of ἐν , en , 'in' and κεφαλή , kephalé , 'head', and the medical suffix -itis 'inflammation'.
Anti-NMDA receptor encephalitis is a type of brain inflammation caused by antibodies. [4] Early symptoms may include fever , headache, and feeling tired. [ 1 ] [ 2 ] This is then typically followed by psychosis which presents with false beliefs (delusions) and seeing or hearing things that others do not see or hear (hallucinations). [ 1 ]
Bickerstaff brainstem encephalitis is a rare inflammatory disorder of the central nervous system, [3] first described by Edwin Bickerstaff in 1951. [ 4 ] [ 5 ] It may also affect the peripheral nervous system , and has features in common with both Miller Fisher syndrome and Guillain–Barré syndrome .
Anti-IgLON5 disease is an uncommon neurological autoimmune condition linked to autoantibodies directed against the IgLON5 protein. [1] Sleep disturbance, bulbar symptoms, and abnormal gait make up the majority of the clinical presentation, which is then followed by cognitive dysfunction. [2]
Acute necrotizing encephalopathy (ANE) or sometimes necrotizing encephalitis or infection-induced acute encephalopathy (IIAE) is a rare type of brain disease (encephalopathy) that occurs following a viral infection. [4] Most commonly, it develops secondary to infection with influenza A, influenza B, and the human herpes virus 6. ANE can be ...