Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia is a rare neurodegenerative disease resulting from mutations in the colony stimulating factor 1 receptor gene. Accurate diagnosis can be difficult because the associated clinical and MR imaging findings are nonspecific. We pres...

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Veröffentlicht in:American journal of neuroradiology : AJNR 2017-01, Vol.38 (1), p.77-83
Hauptverfasser: Konno, T, Broderick, D F, Mezaki, N, Isami, A, Kaneda, D, Tashiro, Y, Tokutake, T, Keegan, B M, Woodruff, B K, Miura, T, Nozaki, H, Nishizawa, M, Onodera, O, Wszolek, Z K, Ikeuchi, T
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Sprache:eng
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Zusammenfassung:Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia is a rare neurodegenerative disease resulting from mutations in the colony stimulating factor 1 receptor gene. Accurate diagnosis can be difficult because the associated clinical and MR imaging findings are nonspecific. We present 9 cases with intracranial calcifications distributed in 2 brain regions: the frontal white matter adjacent to the anterior horns of the lateral ventricles and the parietal subcortical white matter. Thin-section (1-mm) CT scans are particularly helpful in detection due to the small size of the calcifications. These calcifications had a symmetric "stepping stone appearance" in the frontal pericallosal regions, which was clearly visible on reconstructed sagittal CT images. Intrafamilial variability was seen in 2 of the families, and calcifications were seen at birth in a single individual. These characteristic calcification patterns may assist in making a correct diagnosis and may contribute to understanding of the pathogenesis of leukoencephalopathy.
ISSN:0195-6108
1936-959X
DOI:10.3174/ajnr.A4938