Department of Neurology, Hôpital Erasme-ULB, Brussels, Belgium.
J Neuroimaging. 2012 Jul;22(3):308-11. doi: 10.1111/j.1552-6569.2010.00542.x. Epub 2010 Nov 17.
Autoimmune polyglandular syndrome (APS) type 2 (Schmidt syndrome) is a disorder characterized by a combination of autoimmune adrenal insufficiency, autoimmune thyroid disease, and type 1 autoimmune diabetes mellitus. We describe the first case of subacute cerebellar syndrome associated with APS type 2. Brain magnetic resonance imaging showed atrophy of the cerebellum and the vermis, as well as of the anterior pituitary gland. Magnetic resonance spectroscopy showed decreased N-acetylaspartate/creatine ratio in the cerebellum and in the pons. Our findings expand the spectrum of neurological deficits in APS type 2 and underlines that cerebellar pathways may be a main target of the disorder.
自身免疫性多腺体综合征(APS)2 型(施密特综合征)是一种以自身免疫性肾上腺皮质功能减退、自身免疫性甲状腺疾病和 1 型自身免疫性糖尿病合并为特征的疾病。我们描述了首例与 APS 2 型相关的亚急性小脑综合征。脑部磁共振成像显示小脑和蚓部以及前垂体腺萎缩。磁共振波谱显示小脑和脑桥的 N-乙酰天冬氨酸/肌酐比值降低。我们的发现扩展了 APS 2 型的神经缺损谱,并强调小脑通路可能是该疾病的主要靶标。