T1/T2 Isointense Parenchymal Lesions
Anne G. Osborn, MD, FACR
DIFFERENTIAL DIAGNOSIS
Common
Cerebral Ischemia-Infarction, Hyperacute
Intracerebral Hematoma (Hyperacute)
Capillary Telangiectasia
Developmental Venous Anomaly
Meningioma
Less Common
Metastases, Parenchymal
Lymphoma, Primary CNS
Rare but Important
Neurosarcoid
Heterotopic Gray Matter
Tuber Cinereum Hamartoma
Tuberous Sclerosis Complex
Cerebral Infarction, Subacute
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Lesions can be isointense with brain parenchyma generally vs. isointense compared to cortex or white matter
Most comparisons are to gray matter
Very few parenchymal lesions truly isointense to gray matter on both T1/T2WI
FLAIR, PD, DWI may be abnormal when T1/T2WI normal or subtle
T2* GRE helpful in hyperacute hemorrhage
Detects field homogeneities caused by inhomogeneous clot
Detects presence of other lesions (e.g., microhemorrhages)
T1 C+ scans increase sensitivity for small vascular malformations, neoplasms
Lesions that are really, truly isointense to cortex and neither enhance nor restrict are uncommon
Heterotopic gray matter
Tuber cinereum hamartoma
Helpful Clues for Common Diagnoses
Cerebral Ischemia-Infarction, Hyperacute
T1/T2WI typically normal in hyperacute
Look for show subtle signs of gyral swelling, sulcal effacement
FLAIR
Subtle abnormalities may be apparent using narrow windows
Look for “dot sign” (intravascular high signal intensity caused by occlusion/slow flow)
Found in 10% of patients with acute stroke
Intracerebral Hematoma (Hyperacute)
Clot contains intracellular oxyhemoglobin, which is diamagnetic
Although hyperacute clot can be isointense on T1WI, most hematomas are inhomogeneous, often hyperintense on T2WI
Capillary Telangiectasia
Can be anywhere
Pons, medulla > supratentorial cortex, white matter
Imaging
Unless unusually large, typically invisible on T1/T2WI
Use T2* sequence (become hypointense on GRE, SWI)
T1 C+ shows “brush-like” enhancement
May see tiny central draining vein within lesion
Developmental Venous Anomaly
Most common cerebrovascular anomaly
Imaging
If small, often invisible on T1/T2WI
Larger DVAs may have discernible flow void or flow-related enhancement
If slow flow in “Medusa head” (medullary veins), may become hypointense on T2* (GRE/SWI)
Best seen on T1 C+
Meningioma
Not truly a parenchymal lesion although some may invaginate into brain
Included because often isointense to cortex, difficult to detect on nonenhanced T1WI, T2WI
Look for signs of extra-axial location
Gray-white matter “buckling”
CSF-vascular “cleft”
Most enhance on T1 C+
Helpful Clues for Less Common Diagnoses
Metastases, Parenchymal
Most hyperintense on FLAIR, T2WI
Gray-white matter junction distortion
Few are isointense on both T1/T2WI
Most (not all) have detectable edema
Look for subtle alteration in gyral shape, sulcal effacement
Most enhance
Lymphoma, Primary CNS
Hypercellular tumor, high nuclear: cytoplasm ratio
Isointense (cortex, basal ganglia) on both T1/T2WI
Hemorrhage, necrosis rare unless HIV/AIDS
Look for anatomic distortion of deep periventricular structures
Almost always enhances
Helpful Clues for Rare Diagnoses
Neurosarcoid
Can be anywhere, look like almost anything!
Dural-based masses > > parenchymal lesions
Infiltration along perivascular spaces → parenchymal masses
Isointense on T1WI
Typically hyperintense on T2WI, FLAIR
Exception: Lesions in infundibular stalk usually isointense on all sequences
Enhance strongly, sometimes heterogeneously
Heterotopic Gray Matter
Isointense to cortex on all sequences, no enhancement
Can be cortical, subcortical white matter, subependymal
Beware: Masses of heterotopic gray matter can distort ventricle, mimic tumor!
Tuber Cinereum Hamartoma
Typical clinical presentationStay updated, free articles. Join our Telegram channel
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