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

被引:47
作者
Konno, T. [1 ,3 ]
Broderick, D. F. [2 ]
Mezaki, N. [3 ]
Isami, A. [3 ]
Kaneda, D. [6 ,7 ]
Tashiro, Y. [8 ]
Tokutake, T. [3 ]
Keegan, B. M. [9 ]
Woodruff, B. K. [10 ]
Miura, T. [3 ]
Nozaki, H. [5 ]
Nishizawa, M. [3 ]
Onodera, O. [3 ]
Wszolek, Z. K. [1 ]
Ikeuchi, T. [4 ]
机构
[1] Mayo Clin Florida, Dept Neurol, Jacksonville, FL USA
[2] Mayo Clin Florida, Dept Radiol, Jacksonville, FL USA
[3] Niigata Univ, Sch Hlth Sci, Fac Med, Dept Neurol, Niigata, Japan
[4] Niigata Univ, Sch Hlth Sci, Fac Med, Dept Mol Genet,Brain Res Inst, Niigata, Japan
[5] Niigata Univ, Sch Hlth Sci, Fac Med, Dept Med Technol, Niigata, Japan
[6] Tokyo Metropolitan Geriatr Hosp, Dept Neurol, Tokyo, Japan
[7] Osaka Red Cross Hosp, Dept Neurol, Osaka, Japan
[8] Mito Med Ctr, Natl Hosp Org, Dept Neurol, Ibaraki, Japan
[9] Mayo Clin Rochester, Dept Neurol, Rochester, MN USA
[10] Mayo Clin Arizona, Dept Neurol, Scottsdale, AZ USA
基金
美国国家卫生研究院;
关键词
HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY; NEUROAXONAL SPHEROIDS; MULTIPLE-SCLEROSIS; CSF1R MUTATIONS; HDLS; LEUKODYSTROPHY; CALCINOSIS; FEATURES; DISEASE; ENTITY;
D O I
10.3174/ajnr.A4938
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:77 / 83
页数:7
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