Gingold M K, Bodensteiner J B, Schochet S S, Jaynes M
Department of Pediatrics, West Virginia University Health Sciences Center, Morgantown 26506-9180, USA.
J Child Neurol. 1999 May;14(5):325-9. doi: 10.1177/088307389901400510.
Subacute necrotizing encephalomyelopathy (Leigh syndrome) refers to a nebulous disease entity characterized by lactic acidosis, a wide variety a clinical manifestations, and a consistent conglomeration of pathologic findings. Several abnormalities in metabolism have been delineated in association with Leigh syndrome, but many cases have no identified metabolic abnormality. We report a case that clinically, metabolically, and neuroradiologically appeared to be Leigh syndrome. In addition, our patient exhibited other unusual clinical findings, including ocular motility abnormalities. Neuropathologically, however, the diagnosis of Alexander's disease was confirmed. A review of the literature failed to find other cases of Alexander's disease reported with the metabolic abnormalities and clinical manifestations with which our patient presented.
亚急性坏死性脑脊髓病(Leigh综合征)是一种模糊的疾病实体,其特征为乳酸性酸中毒、多种多样的临床表现以及一系列一致的病理表现。与Leigh综合征相关的代谢方面已发现了几种异常情况,但许多病例并未发现明确的代谢异常。我们报告了一例在临床、代谢及神经放射学表现上看似Leigh综合征的病例。此外,我们的患者还表现出其他不寻常的临床发现,包括眼球运动异常。然而,神经病理学检查确诊为亚历山大病。文献回顾未发现有其他亚历山大病病例报告具有我们患者所呈现的代谢异常和临床表现。