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. 2015 Jul 22;17(11):1525–1537. doi: 10.1093/neuonc/nov117

Table 1.

VASARI imaging features

Imaging Features Scoring Value Definition
Major axis NA The longest diameter of the tumor which is based upon measurement of the FLAIR abnormality on a single axial image that demonstrates the largest cross-sectional area.
Minor axis NA The diameter of the FLAIR abnormality which is perpendicular to the longest diameter. The measurement is performed on a single axial image that demonstrates the largest cross-sectional area.
Tumor location Frontal lobe
Temporal lobe
Parietal lobe
Occipital lobe
Insular
Basal ganglia
Thalamus
Brainstem
Cerebellum
Corpus callosum
Location of lesion geographic epicenter, the largest component of the tumor, either contrast-enhancing tumor (CET) or non-contrast-enhancing tumor (nCET).
Nonenhancing tumor (nCET) is defined as regions of T2W hyperintensity (less than the intensity of cerebrospinal fluid, with corresponding T1W hypointensity) that are associated with mass effect and architectural distortion, including blurring of the gray-white interface.
Side of tumor epicenter Right
Center/Bilateral
Left
Side of lesion epicenter irrespective of whether the lesion crosses into the contralateral hemisphere.
Eloquent brain No eloquent brain
Speech motor
Speech receptive
Motor
Vision
Presence of tumor involvement of the eloquent cortex or immediate subcortical white matter of eloquent cortex.
Enhancement quality No contrast enhancement
Mild (when barely discernible but unequivocal degree of enhancement is present relative to precontrast images)
Marked (obvious tissue enhancement).
Qualitative degree of contrast enhancement defined as having all or portions of the tumor that demonstrate significantly higher signal on the postcontrast T1W images compared with precontrast T1W images.
Proportion enhancing <5%, 6%–33%, 34%–67%, 68%–95%, >95% Visually estimated proportion of enhancing component to the entire tumor
Proportion nCET <5%, 6%–33%, 34%–67%, 68%–95%, >95% Visually estimated proportion of nonenhancing component to the entire tumor
Proportion necrosis <5%, 6%–33%, 34%–67%, 68%–95%, >95% Visually estimated proportion of necrosis to the entire tumor.
Necrosis is defined as a region within the tumor that does not enhance, is high on T2W and proton density images, is low on T1W images, and has an irregular border.
Proportion of edema <5%, 6%–33%, 34%–67%, 68%–95%, >95% Visually estimated proportion of edema to the entire tumor.
Edema is defined as a region which is greater in signal than nCET and somewhat lower in signal than CSF. Pseudopods are characteristic of edema.
Cyst(s) Absent OR present Well-defined, rounded, often eccentric regions of very bright T2W signal and low T1W signal essentially matching CSF signal intensity, with very thin, regular, smooth, nonenhancing or regularly enhancing walls, possibly with thin, regular, internal septations.
Multifocal or multicentric Focal
Multifocal or multicentric
Gliomatosis
Multifocal is defined as having at least one region of tumor, either enhancing or nonenhancing, which is not contiguous with the dominant lesion and is outside the region of signal abnormality (edema) surrounding the dominant mass. This can be defined as those resulting from dissemination or growth by an established route, spread via commissural or other pathways, or via CSF channels or local metastases.
Multicentric are widely separated lesions in different lobes or different hemispheres that cannot be attributed to one of the previously mentioned pathways.

Gliomatosis refers to generalized neoplastic transformation of the white matter of most of a hemisphere.
T1/FLAIR ratio Expansive (size of precontrast T1 abnormality approximates size of FLAIR abnormality)
Mixed (size of T1 abnormality moderately less than FLAIR envelope)
Infiltrative (size of precontrast T1 abnormality much smaller than size of FLAIR abnormality)
Gross comparison in the overall lesion size between precontrast T1 and FLAIR (in the same plane). Use T2 if FLAIR is not provided.
Thickness of enhancing margin Thin (<3 mm)
Thick/nodular (>3 mm)
Solid (only solid enhancement, no rim)
The thickness of enhancing margin of the tumor. The scoring is not applicable if there is no contrast enhancement.
Definition of the enhancing margin Well defined
Poorly defined
The definition of the outside margin of the enhancement. The scoring is not applicable if there is no contrast enhancement.
Definition of the nonenhancing margin Well defined
Poorly defined
The definition of the outside margin of the nonenhancing margin of the tumor.
Hemorrhage Yes OR No Intrinsic hemorrhage anywhere in the tumor matrix. Any intrinsic foci of low signal on T2WI or high signal on T1WI.
Diffusion characteristics Facilitated
Restricted
Mixed
Indeterminate
Predominantly facilitated or restricted diffusion in the enhancing or nCET portion of the tumor. (Based on apparent diffusion coefficient [ADC] map) (Rate CET alone when present, otherwise use nCET)
Indeterminate = unsure.
Mixed = relatively equal proportion of facilitated and restricted.
No ADC maps = use no images. Proportion of tissue not relevant.
Pial invasion Yes OR No Enhancement of the overlying pia in continuity with enhancing or nonenhancing tumor.
Ependymal extension Yes OR No Invasion of any adjacent ependymal surface in continuity with enhancing or nonenhancing tumor matrix.
Cortical involvement Yes OR No Nonenhancing or enhancing tumor extending to the cortical mantle or cortex is no longer distinguishable relative to subjacent tumor.
Deep white matter invasion Yes OR No Enhancing or nCET tumor extending into the internal capsule, corpus callosum, or brainstem.
nCET crosses midline Yes OR No nCET crosses into contralateral hemisphere through white matter commissures (exclusive of herniated ipsilateral tissue).
CET crosses midline Yes OR No Enhancing tissue crosses into contralateral hemisphere through white matter commissures (exclusive of herniated ipsilateral tissue).
Satellites Yes OR No An area of enhancement within the region of signal abnormality surrounding the dominant lesion but not contiguous in any part with the major tumor mass.
Calvarial remodeling Yes OR No Erosion of inner table of skull (possibly a secondary sign of slow growth).