Axial T2-weighted (image 1) and susceptibility-weighted (ima | Figure 1

CincyKidsRad

Cincinnati Children's Radiology

Axial T2-weighted (image 1) and susceptibility-weighted (image 2) images show subcortical white matter anomalies (also known as tubers; arrow, image 1) and calcification with susceptibility artifact of one of the subependymal nodules (arrow, image 2). The imaging findings are consistent with tuberous sclerosis. Other neuroimaging findings of tuberous sclerosis include subependymoma giant cell astrocytoma, radial migration lines, and microcephaly. Heterotopic gray matter can also cause subependymoma nodularity. #FridayQuizDay #FridayQuiz


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Axial T1 FLAIR MRI shows subependymal gray matter heterotopia (arrowhead), the most commonly observed form of gray matter heterotopia. The differential diagnosis for this finding includes subependymal nodules that occur in tuberous sclerosis complex. Gray matter heterotopia is distinguished from subependymal nodules of tuberous sclerosis by the signal intensity of the nodule; in tuberous sclerosis, the T2 signal of subependymal nodules is higher than that of normal gray matter while nodules in gray matter heterotopia are isointense to gray matter. Patients with tuberous sclerosis may also have additional stigmata such as subcortical tubers and subependymal giant cell astrocytomas.

Axial susceptibility weighted image in a patient involved in a motor vehicle collision shows multiple foci of signal loss (arrows) at the gray matter/white matter junction. These regions are associated with restricted diffusion (arrows, image 2). Diffuse axonal injury is a traumatic axonal stretch injury associated with sudden deceleration. On imaging, small foci of hemorrhage may be seen at the gray matter/white matter junction.

Axial susceptibility-weighted (image 1), axial T2 (image 2), and axial (image 3) images show marked tortuosity of the intracranial vasculature and abnormal signal within the pulvinar (arrows) and subcortical white matter (arrowhead) consistent with Menkes syndrome. Menkes syndrome is an x-linked recessive disorder of copper metabolism characterized by kinky hair, failure to thrive, and hypotonia. #NeuroWednesday