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Acute inflammatory demyelinating polyradiculoneuropathy (AIDP)
a.k.a. Guillain-Barré syndrome (GBS)
Autoimmune postinfectious or postvaccinial acute inflammatory demyelination of peripheral nerves, nerve roots, cranial nerves
Smooth pial enhancement of cauda equina and conus medullaris
Nerve roots often slightly enlarged
Conus not enlarged
Axial T1WI C+ MR shows preferential contrast accentuation of ventral roots in cauda
Miller-Fischer syndrome
Chronic polyneuropathies
Subacute inflammatory demyelinating polyradiculoneuropathy
Chronic inflammatory demyelinating polyradiculoneuropathy
Hereditary polyneuropathies
Carcinomatous or lymphomatous meningitis
Anterior lumbar radiculopathy
Antecedent event or “trigger” in 70% of GBS cases
Usually follows recent viral illness
Campylobacter jejuni infection can be trigger
Classically presents with “ascending paralysis”
If ascends to brainstem, may involve cranial nerves, require ventilator
Sensory loss common but less severe
Cerebrospinal fluid shows albuminocytologic dissociation (↑ protein in absence of elevated WBCs)
Guillain-Barré syndrome (GBS)
Acute inflammatory demyelinating polyradiculoneuropathy (AIDP)
“Ascending paralysis”
Autoimmune postinfectious or postvaccinial acute inflammatory demyelination of peripheral nerves, nerve roots, cranial nerves
Best diagnostic clue
Smooth pial enhancement of cauda equina and conus medullaris
Location
On imaging, typically cauda equina, especially ventral roots
Size
Nerve roots may be slightly enlarged
Morphology
Symmetric, smooth appearance of roots
CECT
May see symmetric enhancement of lumbar roots
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