Conventional and advanced MR imaging in infantile Refsum disease

被引:0
|
作者
Kilic, Mustafa [1 ]
Karli-Oguz, Kader [3 ]
Haliloglu, Goknur [2 ]
Topcu, Meral [2 ]
Wanders, Ronald James [4 ]
Coskun, Turgay [1 ]
机构
[1] Hacettepe Univ, Fac Med, Div Pediat Nutr & Metab, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Fac Med, Div Pediat Neurol, Dept Pediat, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Fac Med, Dept Radiol, TR-06100 Ankara, Turkey
[4] Univ Amsterdam, Acad Med Ctr, Lab Genet Metab Dis, Dept Pediat, NL-1105 AZ Amsterdam, Netherlands
关键词
infantile Refsum disease; cranial MRI; MRS; X-LINKED-ADRENOLEUKODYSTROPHY; PEROXISOME BIOGENESIS; ZELLWEGER-SYNDROME; DISORDERS; SPECTROSCOPY; LEUKODYSTROPHIES; TRANSPLANTATION; DYSFUNCTION; DEFICIENCY; AMAUROSIS;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report magnetic resonance (MR) imaging findings including diffusion-weighted imaging and proton MR spectroscopy findings in a patient with infantile Refsum disease. The initial diagnosis was made on the basis of history, clinical findings and biochemical studies. Bilateral and symmetrical involvement of the peritrigonal white matter, centrum semiovale, thalami, corpus callosum and corticospinal tracts as assessed by increased T2 signal was highly suggestive of a peroxisomal disorder. Facilitated diffusion was observed in diseased parenchyma. Long echo-time (TE: 270 ms) MRS showed decreased N-acetyl-aspartate/creatine and elevated choline/creatine and lactate; short echo-time MRS (TE: 30 ms) revealed increased myoinositol at 3.56 ppm and lipid peaks at 0.9 and 1.3 ppm. A major contribution to the differential diagnosis came from MR imaging and proton MRS, as discussed in this report.
引用
收藏
页码:294 / 299
页数:6
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