Perivascular Space Enhancing Lesions
Karen L. Salzman, MD
DIFFERENTIAL DIAGNOSIS
Common
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Meningitis
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Neurosarcoid
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Tuberculosis
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Vasculitis
Less Common
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Glioblastoma Multiforme
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Lymphoma, Intravascular (Angiocentric)
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Cerebral Amyloid Disease
Rare but Important
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Metastases
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Granulomatous Angiitis
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Langerhans Cell Histiocytosis
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Wegener Granulomatosis, Brain
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Moyamoya (Mimic)
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Meningioangiomatosis
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Neurocutaneous Melanosis
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
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Perivascular spaces (PVS) are pial-lined, fluid-filled structures that accompany penetrating arteries
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PVS follow CSF on all MR sequences
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Rarely an enhancing vessel may be seen centrally within the PVS as a normal variant
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Enhancement of PVS is typically related to infection, vasculitis, or tumor
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Age of patient may help differentiate lesions
Helpful Clues for Common Diagnoses
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Meningitis
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Enhancing leptomeninges typical
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Hydrocephalus very common
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Inflammatory cells may extend along PVS
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More common in children
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May cause an infectious vasculitis; infarction due to vasculitis in 25%
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Neurosarcoid
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Multisystem inflammatory disease characterized by noncaseating granulomas
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Meningeal enhancement typical (leptomeningeal & dural)
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May invade brain via PVS & cause diffuse or focal mass-like lesions
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Periventricular T2 hyperintense lesions common (50%)
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May cause a small vessel vasculitis (involves penetrating arteries)
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Tuberculosis
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Meningitis + parenchymal lesions common appearance
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Inflammatory cells may extend along PVS
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May cause an infectious vasculitis
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Skull base vessels most commonly involved (supraclinoid ICA & M1)
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Vasculitis
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Heterogeneous group of CNS disorders with inflammation & blood vessel necrosis
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Primary or secondary to systemic disease
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Alternating stenosis, dilatation primarily involving 2nd, 3rd order branches
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Angiography best for diagnosis
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Multifocal ischemia in subcortical white matter (WM) & basal ganglia (BG)
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May cause PVS enhancement
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Helpful Clues for Less Common Diagnoses
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Glioblastoma Multiforme
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Peripherally enhancing, centrally necrotic WM mass typical
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Often involves corpus callosum
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May metastasize along PVS
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Lymphoma, Intravascular (Angiocentric)
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Rare malignancy characterized by intravascular proliferation of lymphoid cells with a predilection for CNS & skin
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Multifocal T2 hyperintensity in deep WM, cortex, or BG + enhancement typical
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May see cortical infarct-like lesions
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May cause a vasculitis
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Cerebral Amyloid Disease
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Lobar hemorrhages of different ages & multifocal “black dots” typical
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Amyloid deposits may occur along PVS
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May cause a vasculitis
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Occurs in elderly adults
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Helpful Clues for Rare Diagnoses
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Metastases
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Multifocal parenchymal enhancement at gray-white interfaces typical
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May rarely spread along PVS or involve meninges
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Primary tumor often known
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Granulomatous Angiitis
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Primary angiitis isolated to the CNS (idiopathic)
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Manifests as multiple intracranial stenoses
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May cause PVS enhancement in BG or WM
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Langerhans Cell Histiocytosis
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Thick enhancing pituitary stalk is most common CNS manifestation
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Lack of pituitary “bright spot”
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May extend along PVS
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Rarely causes enhancing choroid plexus, BG, &/or leptomeningeal nodules
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Wegener Granulomatosis, Brain
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Chronic systemic arteritis involving lungs, kidneys, & sinuses
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CNS involved in 15-30% due to direct invasion from nose/sinuses
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May cause intracerebral & meningeal granulomas or vasculitis
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May cause meningeal & PVS enhancement
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Moyamoya (Mimic)
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Moyamoya is an angiographic pattern
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Idiopathic progressive arteriopathy of childhood
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Slowly progressive occlusion of the supraclinoid ICAs
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T2 MR shows multiple dark flow voids in BG related to lenticulostriate collaterals
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Contrast MR shows enhancement of these collaterals mimicking PVS enhancement
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