Anterior temporal white matter lesions in myotonic dystrophy with intellectual impairment : an MRI and neuropathological study

• Published in: Neuroradiology 1998-07, Vol.40 (7), p.411-415
• Main Authors: OGATA, A, TERAE, S, FUJITA, M, TASHIRO, K
• Format: Article
• Language: English
• Subjects: Adult; Biological and medical sciences; Cognition Disorders - diagnosis; Cognition Disorders - etiology; Diseases of striated muscles. Neuromuscular diseases; Female; Humans; Magnetic Resonance Imaging; Male; Medical sciences; Mental Status Schedule; Myotonic Dystrophy - pathology; Myotonic Dystrophy - psychology; Neurology; Temporal Lobe - pathology
• ISSN: 0028-3940; 1432-1920
• DOI: 10.1007/s002340050613

We studied 12 patients with myotonic dystrophy using MRI and the Mini-mental state examination (MMSE), to see it specific MRI findings were associated with intellectual impairment. We also compared them with the neuropathological findings in an autopsy case of MD with intellectual impairment. Mild intellectual impairment was found in 8 of the 12 patients. On T2-weighted and proton density-weighted images, high-intensity areas were seen in cerebral white matter in 10 of the 12 patients. In seven of these, anterior temporal white-matter lesions (ATWML) were found; all seven had mild intellectual impairment (MMSE 22-26), whereas none of the four patients with normal mentation had ATWML. In only one of the eight patients with intellectual impairment were white-matter lesions not found. Pathological findings were severe loss and disordered arrangement of myelin sheaths and axons in addition to heterotopic neurons within anterior temporal white matter. Bilateral ATWML might be a factor for intellectual impairment in MD. The retrospective pathological study raised the possibility that the ATWML are compatible with focal dysplasia of white matter.