Teaching NeuroImages: T2 hyperintensities in neurofibromatosis type 1.
case_report · Level V
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- Record sourced from PubMed, PMID 23671349.
- Also identified by DOI 10.1212/WNL.0b013e3182929f7c and PMC identifier 3908353.
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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.
Medical subject headings
- Magnetic Resonance Imaging
- Neurofibromatosis 1
- Optic Nerve Glioma