| Literature DB >> 27633805 |
T Konno1,2, D F Broderick3, N Mezaki2, A Isami2, D Kaneda4,5, Y Tashiro6, T Tokutake2, B M Keegan7, B K Woodruff8, T Miura2, H Nozaki9, M Nishizawa2, O Onodera2, Z K Wszolek1, T Ikeuchi10.
Abstract
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.Entities:
Mesh:
Year: 2016 PMID: 27633805 PMCID: PMC5233547 DOI: 10.3174/ajnr.A4938
Source DB: PubMed Journal: AJNR Am J Neuroradiol ISSN: 0195-6108 Impact factor: 3.825