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Adult cerebral adrenoleukodystrophy and Addison's disease in a female carrier
Authors:Xiaoyan Chen  Zhiye Chen  Dehui Huang  Xiaofeng Liu  Qiuping Gui  Shengyuan Yu
Institution:1. Department of Neurology, Chinese PLA General Hospital, Beijing, China;2. Department of Radiology, Chinese PLA General Hospital, Beijing, China;3. Department of Pathology, Chinese PLA General Hospital, Beijing, China;4. Department of Neurology, Chinese PLA General Hospital, No. 28, Fuxing Road, Beijing 100853, China
Abstract:We described a 38-year-old woman of rapidly progressive dementia with white matter encephalopathy and death. She had Addison's disease but the adrenal glands were hyperplastic. Brain magnetic resonance imaging revealed diffuse white matter lesion predominantly in the frontal lobe with band-like contrast enhancement. l-Methyl-11C-methionine positron emission tomography revealed accumulation of tracer in bilateral frontal lobes. Stereotactic biopsy demonstrated demyelination changes. A number of urinary organic acids were elevated. Adrenoleukodystrophy was diagnosed by elevated plasma very long chain fatty acid and ABCD1 gene mutation (C1544C/T). Adrenoleukodystrophy should be considered as a differential diagnosis in women with rapidly progressive white matter encephalopathy.
Keywords:X-ALD  X-linked adrenoleukodystrophy  VLCFA  very long chain fatty acid  MRI  magnetic resonance imaging  ACTH  adrenocorticotropic hormone  ENA  anti-extractable nuclear antigens  DWI  diffusion weighted imaging  MRS  magnetic resonance spectroscopy  Cho/NAA  choline/N-acetyl aspartate  11C-MET PET  l-methyl-11C-methionine positron emission tomography  CT  computed tomography
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