Dietemann J L, Filippi de la Palavesa M M, Tranchant C, Kastler B
Service de Radiologie Médico-Chirurgicale B, Hôpital Central, Strasbourg, France.
Neuroradiology. 1990;32(6):485-7. doi: 10.1007/BF02426460.
MR findings are reported in three patients presenting mannosidosis. Among a family of 8 children, 4 presented typical clinical and biological abnormalities related to mannosidosis. Brain MR examinations including sagittal T1 and axial T2 sections were obtained in three patients of this family (one 25-year-old male, one 34-year-old female, and one 35-year-old female). MR scans demonstrate seven types of modifications: (1) brachycephaly, (2) thick calvaria, (3) verticalization of the chiasmatic sulcus, (4) poor pneumatization of the sphenoid body, (5) partial empty sella turcica (6) cerebellar atrophy, and (7) white matter signal modifications. High signal abnormalities involving the parieto-occipital white matter are identified on axial T2-weighted scans in the three patients and are probably related to demyelination and associated gliosis as described previously by several authors on specimens.
报告了3例患有甘露糖苷贮积症患者的磁共振成像(MR)检查结果。在一个有8个孩子的家庭中,4名儿童表现出与甘露糖苷贮积症相关的典型临床和生物学异常。对该家庭中的3名患者(1名25岁男性、1名34岁女性和1名35岁女性)进行了脑部MR检查,包括矢状位T1和轴位T2扫描。MR扫描显示出7种类型的改变:(1)短头畸形;(2)颅骨增厚;(3)视交叉沟垂直化;(4)蝶骨体气化不良;(5)部分蝶鞍空泡;(6)小脑萎缩;(7)白质信号改变。在3例患者的轴位T2加权扫描上均发现涉及顶枕白质的高信号异常,这可能与脱髓鞘及相关的胶质增生有关,此前已有多位作者在标本上描述过这种情况。