MR Imaging (Basics)
General:
- fat is always bright (except modified sequences like STIR)
General:
- fat is always bright (except modified sequences like STIR)
- bone is always dark
- marrow is somewhere in between
T1:
- anatomy scans (resolution of normal anatomy good)
- things that are bright on T1: fat, subacute blood (=metHb), melanin, contrast.
- things that are bright on T1: fat, subacute blood (=metHb), melanin, contrast.
- fluid is dark on T1
- protip: T1 noncon is a good way to look for recent bleed (days to ~2-3 weeks) if you don't have GRE imaging.
- protip: T1 noncon is a good way to look for recent bleed (days to ~2-3 weeks) if you don't have GRE imaging.
T2
- Fluid is bright
- FLAIR = T2 with CSF subtracted out.
- In cases of bleeds, intact RBC membrane acts as a local magnet, and will appear dark on T2.
Blood on MR:
- In cases of bleeds, intact RBC membrane acts as a local magnet, and will appear dark on T2.
Blood on MR:
Time course | Substrate | T1 | T2 |
Hyperacute | Intracellular oxyhemoglobin | Iso | Iso-br |
Acute (hrs-days) | Intracellular deoxyhemoglobin | Iso | Dark |
Early subacute (days-wks) | Intraceullar methemoglobin | Bright | Dark |
Late subacute | Extracellular methemoglobin | Bright | Bright |
Remote | Ferritin/hemosiderin | Dark | Dark |
DWI
- restriction in mobility of water molecules (brownian motion)
- restricted diffusion shows up bright = cytotoxic edema
- ischemia leads to failure of membrane ion pumps; cells swell with fluid; water that used to be in the extracellular space is now in the cell, which limits its motion
- most common cause of cytotoxic edema is ischemia, but there are other pathologies: necrosis (abscess, tumor center, radiation damage), epidermoid tumor, acute demyelination, acute encephalitis, CJD, tumors with high nuclear:cytoplasmic ratio, elevated protein or subacute blood
- T2 shine through: DWI is a T2-derived study, lesions that are bright on T2 (ie tumors) will be bright on DWI as well; thus we use the the apparent diffusion coefficient (calculated from T2) to showcase intrinsically T2-bright things
- theoretically, DWI changes appear as early as 6 mins after ischemic insult and as late as 2 weeks after; imaging changes will be apparent on ADC (dark) before they are apparent on DWI
- ADC-dark lesions will eventually become bright over time as the cells complete necrosis
- T2 shine through: DWI is a T2-derived study, lesions that are bright on T2 (ie tumors) will be bright on DWI as well; thus we use the the apparent diffusion coefficient (calculated from T2) to showcase intrinsically T2-bright things
- theoretically, DWI changes appear as early as 6 mins after ischemic insult and as late as 2 weeks after; imaging changes will be apparent on ADC (dark) before they are apparent on DWI
- ADC-dark lesions will eventually become bright over time as the cells complete necrosis
Gradient recalled echo/susceptibility weighted imaging
- takes advantage of paramagnetic qualities of deoxyhemoglobin and hemosiderin to detect blood products
- most sensitive imaging modality for blood
- most sensitive imaging modality for blood
Contrast
- When to use: refine diagnosis, see small images.
- Things with no BBB that enhance: Pituitatry, hypothalamus, pineal gland, choroid plexus.
MR patterns:
- Dural-based extraaxial mass: meningioma, dural met, granulomatous disease (sarcoid)
- Periventricular ischemia: small vessel disease, watershed infarct
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