Brain MRI Recognition Pattern
Systematic approach to interpreting brain MRI with sequences, anatomical landmarks, and key pathological patterns
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Download Radiology Assistant App1. MRI Sequences
A. Standard Sequences
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T1-weighted:
- Anatomical detail
- Hypointense CSF, gray/white matter differentiation
- Contrast-enhancing lesions (post-gadolinium) -
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T2-weighted:
- Pathological changes
- Hyperintense CSF, edema, tumors
- White matter lesions -
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FLAIR:
- Suppresses CSF signal
- Highlights periventricular lesions
- MS plaques, infarcts -
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DWI/ADC:
- Acute ischemia (bright on DWI, dark on ADC)
- Abscesses, cytotoxic edema -
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SWI/GRE:
- Blood products, calcifications
- Microbleeds, cavernomas
B. Advanced Sequences
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MRA:
- Vascular anatomy
- Aneurysms, stenoses -
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MRV:
- Venous sinuses
- Thrombosis -
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Perfusion:
- rCBV maps
- Tumor grading, penumbra -
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Spectroscopy:
- Metabolic profiles
- Choline/NAA ratio for tumors
2. ABCDEF Systematic Approach
3. Pathological Patterns
A. White Matter Lesions
B. Mass Lesions
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Glioblastoma:
- Irregular ring enhancement
- Central necrosis
- Surrounding FLAIR hyperintensity -
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Meningioma:
- Dural-based
- Homogeneous enhancement
- Dural tail -
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Metastasis:
- Multiple
- Gray-white junction
- Vasogenic edema
4. Vascular Patterns
A. Stroke
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Acute:
- DWI bright (minutes)
- ADC dark (1-7 days)
- T2/FLAIR positive (6-12 hrs) -
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Subacute:
- T1 shortening (3-7 days)
- Gyral enhancement (days-weeks) -
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Chronic:
- Encephalomalacia
- Hemosiderin (GRE hypointense)
B. Hemorrhage Evolution
5. Key Anatomical Landmarks
6. Brain MRI Reporting Template
- 1. Technique: Sequences, contrast use
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2.
Parenchyma:
- Gray/white differentiation
- Focal abnormalities -
3.
Ventricles/Cisterns:
- Size
- Symmetry -
4.
Vascular:
- Flow voids
- Abnormal enhancement -
5.
Bones/Sinuses:
- Fractures
- Sinus disease -
6.
Impression:
- Key findings
- Differential diagnosis
Always correlate with clinical history and prior imaging. Review all sequences systematically. For stroke protocols, check DWI immediately. In trauma, review SWI for microbleeds. For tumors, assess perfusion and spectroscopy when available. Document incidental findings (e.g., aneurysms, empty sella) with appropriate follow-up recommendations. Compare with prior studies for interval changes when possible.
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