Magnetic Resonance Imaging (MRI)
|
|
T1 |
T2 |
DWI |
|
Fluid
(Urine, CSF) |
Dark |
Light |
Dark |
|
Muscle |
Grey |
Grey |
|
|
Fat |
Light |
Light |
|
|
Brain –
Grey matter |
Grey |
Grey |
Grey |
|
Brain –
White matter |
Light grey |
Dark grey |
Light grey |
|
Methaemaglobin |
Light |
Dark or
light |
|
|
Melanin |
Light |
|
|
|
Proteinaceous
fluid |
Light |
|
|
|
|
|
|
|
|
|
T1 |
T2 |
DWI |
ADC |
Contrast |
SWI |
|
Early
hyperacute |
N |
N |
Bright |
Dark |
Nil |
N |
|
Late
hyperacute (>6hours) |
N |
Bright + |
Bright |
Dark |
Mild
enhancement |
N |
|
Acute |
Reduced
(after 16hrs) |
Bright ++ |
Bright |
Returning
to normal |
Enhancement
(>5days) |
Microhaemorrhage |
|
Subacute |
Reduced |
Bright ++ (May get
fogging ~D10) |
Bright |
Normal
(day 10-15) then Bright |
Enhancement |
|
|
Chronic |
Reduced |
Bright ++ |
Bright –
returning to normal |
Bright |
Enhancement
for 2-4 months |
|
|
Stage |
Time |
Blood products |
CT |
T1 |
T2 |
DWI |
ADC |
T2* |
|
Hyperacute |
<24hrs |
Oxy-Hb |
Hyper |
Iso |
Bright |
Bright |
Dark |
Rim bloom |
|
Acute |
1-3days |
Deoxy-Hb |
Hyper |
Iso |
Dark |
Dark |
Dark |
Bloom |
|
Early
subacute |
>3d-1wk |
Intracel. Met-Hb |
Iso |
Bright |
Dark |
Dark |
Dark |
Very dark |
|
Late
subacute |
1wk-mths |
Extracel. Met Hb |
Hypo |
Bright |
Bright |
Bright |
Dark |
Dark rim, variable centre |
|
Chronic |
>14days |
Haemosiderin |
Hypo |
Dark |
Dark |
Dark |
Dark |
Dark |
·
Stroke
o Increasing
intensity during first week then slow resolution occurs over up to 72days
o Almost
100% sensitive – rare cases of missed CVA, thought to be due to initial
sub-occlusive thrombus.
o Almost
100% specific (see below)
o ADC
§ Initially
dark
§ By
5-7 days returns to normal intensity (definitely by 7-10 days)
·
Tumours – Glioma
o May
be hyper, hypo or iosdense on DWI
o If
increased signal it is usually minor and non-specific
·
Tumours – Mets
o May
be hyper, hypo or iosdense on DWI – rarely
hyperintense
o If
there is a necrotic core it is usually strongly hypointense on DWI
·
Tumours – Meningiomas
o Benign
– usually isointense
o Malignant
– often hyperintense
·
Tumours – Lymphoma
o Generally
hyperintense
·
Abscess
o Usually
hyperintense
o ADC
§ Usually
hypointense, often far more so than stroke which may help with differentiation
·
Herpes Encephalitis
o Hyperintense
with low ADC
·
Haemorrhage
·
MS
o New,
contrast enhancing lesions are often - Hyperintense
o Old
lesions are often isointense
o ADC
values often increased indicative of T2 shine through
·
Sustained seizure activity
o Cortical and media thalamic DWI abnormality can occur