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2. MR spectroscopy provides a measure of brain
chemistry. The most common nuclei that are
used are
1
H (proton), 23
Na (sodium), 31
P (phosphorus).
Proton spectroscopy is easier to perform.
3. MRS can be performed within 10-15 minutes and
can be added on to conventional MR imaging
protocols.
It can be used to serially monitor biochemical
changes in tumors, stroke, epilepsy, metabolic
disorders, infections, and neurodegenerative
diseases.
They require interpretation and should always
be correlated with the MR images before
making a final diagnosis.
4. MR spectroscopy is conducted on the same
machine as conventional MRI.
Spectroscopy is a series of tests that are
added to the MRI scan of brain or spine to
measure the chemical metabolism of a
suspected lesion.
There are several different metabolites, or
products of metabolism, that can be
measured to differentiate between tumor
types.
5.
6.
7. Each metabolite appears at a specific ppm, and
each one reflects specific cellular and
biochemical processes
NAA is a neuronal marker and decreases with
any disease that adversely affects neuronal
integrity.
Creatine provides a measure of energy stores.
Choline is a measure of increased cellular
turnover and is elevated in tumors and
inflammatory processes.
8. The common way to analyze clinical spectra
is to look at metabolite ratios, namely
NAA/Cr, NAA/Cho, and Cho/Cr.
9.
10. For MR imaging, the total signal from all the
protons in each voxel is used to make the image.
If all the signal were used for MRS, the fat and
water peaks would be huge and scaling would
make the other metabolite peaks invisible.
Fat and water are eliminated.
Fat is avoided by placing the voxel for MRS
within the brain, away from the fat in bone
marrow and scalp.
11. SINGLE-VOXEL MR
SPECTROSCOPY
Less advance.
Volume averaging
Small area of coverage.
acquires spectra from
single small voxel.
short acquisition times.
Histologically simpler
lesions.
MR SPECTROSCOPIC
IMAGING/MULTI-VOXEL.
more technically advanced
technique.
small voxel size dec.
volume averaging
large volume of coverage
acquires spectra from
numerous small voxels.
long acquisition times.
For complex lesions
12. Multi-voxel spectroscopy is best to detect
infiltration of malignant cells beyond the
enhancing margins of tumors.
Finally, MRS can direct the surgeon to the
most metabolically active part of the tumor
for biopsy to obtain accurate grading of the
malignancy.
13. As a general rule, the single voxel, short TE
technique is used to make the initial
diagnosis.
Multi-voxel, long TE techniques are used to
further characterize different regions of a
mass and to assess brain parenchyma around
or adjacent to the mass.
Multi-voxel, long TE techniques are also used
to assess response to therapy and to search
for tumor recurrence.
14.
15.
MRS can be used to determine the degree of malignancy.
As malignancy increases, NAA and creatine decrease, and
choline, lactate, and lipids increase.
NAA decreases as tumor growth displaces or destroys
neurons.
Very malignant tumors have high metabolic activity and
deplete the energy stores, resulting in reduced creatine.
Very hypercellular tumors with rapid growth elevate the
choline levels.
Lipids are found in necrotic portions of tumors
Lactate appears when tumors outgrow their blood supply
and start utilizing anaerobic glycolysis.
16. Key feature of gliomas is elevated choline
beyond the margin of enhancement due to
infiltration of tumor into the adjacent brain
tissue.
Elevated alanine is a signature of
meningiomas.
17.
Axial enhanced T1-weighted MR image reveals focal enhancement in the left cerebral
peduncle and thalamus. Spectroscopy voxel is placed at the anterior margin of
enhancement.
B, MR spectrum reveals elevation of the Cho/Cr ratio, elevation of the lipid/lactate peak,
and marked reduction of NAA. The pattern was interpreted as consistent with tumor and
was proved to be a glioblastoma multiforme at biopsy.
18. : 58-year-old man with a new right frontal lobe mass.
A, Axial T1-weighted MR image reveals a multilobular cystic and solid mass in the right
frontal lobe that contains peripheral and central enhancing regions. The spectroscopy voxel
is positioned centrally in an enhancing portion of the tumor and does not include the
enhancing edge.
B, MR spectrum reveals absence of discernible Cho, Cr, and NAA. The pattern was thought
to be consistent with no tumor. The lesion was histologically shown to be a glioblastoma
multiforme after resection.
19. Voxel placement in single-voxel MR
spectroscopy studies of brain tumors is critical to
the accurate characterization of lesion
histopathology.
Specifically, inclusion of the edge of an
enhancing lesion in the MR spectroscopy voxel
improves accuracy .
Voxel placement in the centre of a lesion with
frank cavitation increases the likelihood that
cellular breakdown products will dominate the
spectral pattern.
20. To get an accurate assessment of the tumor
chemistry, the spectroscopic voxel should be
placed over an enhancing region of the
tumor, avoiding areas of necrosis,
hemorrhage, calcification, or cysts.
21. A common clinical problem is distinguishing
tumor recurrence from radiation effects
several months following surgery and
radiation therapy.
Elevated choline is a marker for recurrent
tumor. Radiation change generally exhibits
low NAA, creatine, and choline on
spectroscopy.
If radiation necrosis is present, the spectrum
may reveal elevated lipids and lactate.
22. Patient 2: 48-year-old woman with a history of a glioblastoma multiforme treated with
surgery, external beam radiation (59 Gy), and interstitial brachytherapy (58 Gy).
A, Axial T1-weighted MR image reveals enhancement of a right frontal lobe/insular lesion
that has both solid and cavitary components. The spectroscopy voxel includes the medial
margin of enhancement.
B, MR spectrum shows a prominent lipid/lactate peak with minimal residual Cho and Cr; NAA
is absent. The pattern was thought to be consistent with radiation necrosis, and this
diagnosis was confirmed at resection.
23. MRS in a patient with a history of anaplastic astrocytoma treated with surgery and
radiation.
An elevation of the choline (Cho) peak relative to the creatine and N-acetyl asparate (NAA)
peaks and the presence of lactate (Lac) are consistent with recurrent tumor.
24. When the brain becomes ischemic, it
switches to anaerobic glycolysis and lactate
accumulates.
Markedly elevated lactate is the key
spectroscopic feature of cerebral hypoxia and
ischemia.
If cerebral infarction ensues, lipids increase.
25. MR spectroscopy is not routinely used in the
acute setting of head injuries.
when the patient has stabilized, MRS is helpful
to assess the degree of neuronal injury and
predict patient outcomes.
In the case of diffuse axonal injury, imaging
often underestimates the degree of brain
damage.
Clinical outcome correlates inversely with the
NAA/Cr ratio.
The presence of any lactate or lipid indicates a
worse prognosis.
26. Brain abscesses destroy or displace brain
tissue, so NAA is not present.
The voxel should include the abscess cavity to
detect the breakdown products of these
lesions.
Lactate,succinate, alanine, and acetate are
characteristic metabolites in bacterial
abscesses.
Toxoplasmosis and tuberculomas show
prominent peaks from lactate and lipids.
27. Proton magnetic resonance spectroscopy in a treated abscess. (A) Localization of a voxel
in a patient with a pyogenic abscess during the course of antibiotic therapy. (B) The
marked elevation of the isolated lactate (Lac) peak is consistent with a treated abscess. A
similar spectrum would be expected in a cystic or necrotic neoplasm. In an untreated
abscess, the detection of bacterial metabolites such as acetate and succinate would
distinguish abscess from cystic or necrotic neoplasm.
28. Extent of NAA depletion correlates directly with
the degree of dementia in AIDS.
MRS distinguishes the common focal brain
lesions in AIDS patients.
Choline Elevated in lymphoma
Decreased in toxoplasmosis,
tuberuloma cryptococcoma.
Lactate and lipidselevated in toxoplasmosis
Lactate Decreased in Tuberculoma and
cryptococcoma.
29. Magnetic resonance spectroscopy (MRS) is
non invasive means of characterising the
tissue.
Multi-voxel technique more complex but
accurate
MRS highly sensitive but sometimes non
specific
MRS is to be reported in conjunction with
conventional MR.