Gass A, Birtsch G, Olster M, Schwartz A, Hennerici M G
Neurologische Universitätsklinik, Klinikum Mannheim, Universität Heidelberg, Germany.
J Comput Assist Tomogr. 1998 May-Jun;22(3):503-4. doi: 10.1097/00004728-199805000-00026.
Marchiafava-Bignami disease (MBD) was diagnosed in a malnourished 43-year-old patient with chronic alcoholism, severe generalized extrapyramidal rigid syndrome, and severe dyspraxia. Cranial CT and MRI demonstrated isolated lesions in the geno and splenium of the corpus callosum (CC) characteristic for MBD. On thiamine therapy, a slow but steady recovery of clinical symptoms occurred, and serial CT and MRI studies demonstrated marked reversibility of abnormalities in the CC. Besides clinical improvement with a good functional outcome, reversal of CT and MRI abnormalities may occur in MBD.
马尔恰法瓦-比尼亚米病(MBD)在一名43岁营养不良、患有慢性酒精中毒、严重全身性锥体外系僵硬综合征和严重运动障碍的患者中被诊断出来。头颅CT和MRI显示胼胝体(CC)膝部和压部有孤立性病变,这是MBD的特征性表现。在接受硫胺素治疗后,临床症状缓慢但稳步恢复,系列CT和MRI研究显示CC的异常有明显的可逆性。除了临床改善且功能预后良好外,MBD的CT和MRI异常也可能会逆转。