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Other researchers have reported that MR imaging has low specificity in differentiation between benign and malignant masses, and most lesions demonstrate a nonspecific appearance [ 5].
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No specific imaging features alone are capable of differentiating among these various tumours, although most of these lesions demonstrate a higher rate of cystic changes compared with germinomas (Figs. 8 and 9) [26].
Most plexiform lesions demonstrated a weak immunoreactivity of EGFR, which appeared to be located in subendothelial stromal cells.
24 Healed lesions demonstrate hyperpigmented scar tissue.
Skin lesions demonstrate acid fast bacilli on histological analysis.
The lesions demonstrate similar cytologic features seen with Spitz nevi.
AIS lesions demonstrate a very slow growth rate.
That is, lesions receiving a high dose and demonstrating a significant response; lesions receiving a low dose and demonstrating a poor response; lesions receiving a medial dose with a low CoV and demonstrating a significant response; lesions receiving a medial dose with a high CoV and demonstrating a poor response; and lesions demonstrating a poor response despite a high dose being received.
These include hypointense T1-weighted lesions and hyperintense lesions demonstrated on T2-weighted and FLAIR images.
The additional lesions demonstrated signal intensity and enhancement characteristics identical to those of the index lesion.
If follow-up imaging is chosen, it is important to be aware that although most lesions remain stable, a minority may demonstrate an increase or decrease in size over time[ 60, 65, 103 ].
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