Teaching NeuroImages: T2 hyperintensities in neurofibromatosis type 1.

Ostendorf, Adam P; McKinstry, Robert C; Shimony, Joshua S; Gutmann, David H · Neurology · 2013

case_report · Level V

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Abstract

A 4-year-old boy with neurofibromatosis type 1 (NF1), an asymptomatic optic glioma, and a right basal ganglia T2-hyperintense lesion (figure, A and B) developed a left hemiparesis with hyperreflexia over the course of a year. Neuroimaging revealed a cyst-like mass in the region of his previously identified T2 hyperintensity (figure, C and D). While it is often difficult to distinguish T2 hyperintensities from low-grade glioma without tissue diagnosis,<sup>1</sup> even with advanced imaging methods,<sup>2</sup> T2 hyperintensities typically disappear with age and do not become cystic with associated mass effect. Coupled with the development of new neurologic signs, these MRI features are worrisome for neoplasm in a patient with NF1.

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