Schaumburg H H, Powers J M, Raine C S, Spencer P S, Griffin J W, Prineas J W, Boehme D M
Neurology. 1977 Dec;27(12):1114-9. doi: 10.1212/wnl.27.12.1114.
Histopathologic features were studied in postmortem examination of two men with adrenomyeloneuropathy, and biochemical studies were performed on one of these individuals. The histopathologic picture of one case included dying-back features in the nervous system and lamellar cytoplasmic inclusions in the brain, adrenal gland, and testis similar to those in adrenoleukodystrophy. Biochemical studies of the cerebral white matter of this individual revealed increased amounts of long-chain saturated fatty acids in cholesterol esters, an abnormality characteristic of adrenoleukodystrophy. Despite differences in clinical presentation and neuropathology, adrenomyeloneuropathy probably represents a distinct variant of adrenoleukodystrophy.
对两名肾上腺脑白质营养不良症患者进行了尸检,研究其组织病理学特征,并对其中一名患者进行了生化研究。其中一例的组织病理学表现包括神经系统的逆行性变性特征以及大脑、肾上腺和睾丸中的板层状胞质内含物,类似于肾上腺脑白质营养不良症中的表现。对该患者脑白质的生化研究显示,胆固醇酯中的长链饱和脂肪酸含量增加,这是肾上腺脑白质营养不良症的一个特征性异常。尽管临床表现和神经病理学存在差异,但肾上腺脊髓神经病可能是肾上腺脑白质营养不良症的一种独特变体。