Potz G, Neundörfer B
J Neurol. 1975 Oct 24;210(4):283-9. doi: 10.1007/BF00316529.
The case of a patient with a pluripotential immuneproliferative syndrome is reported. She suffered from Hashimoto's thyroiditis with secondary cold agglutination disease and from polyradicular neuritis. Polyradicular neuritis with albumino-cytological dissociation in the CSF had developed chronically and improved only when corticosteroid therapy was begun. Based on this case report fundamental considerations concerning the pathogenesis and therapy of Landry-Guillain-Barre-tstrohl syndrome are discussed.
报告了一例具有多潜能免疫增殖综合征的患者。她患有桥本甲状腺炎并继发冷凝集素病以及多神经根神经炎。脑脊液中存在蛋白细胞分离的多神经根神经炎呈慢性发展,仅在开始使用皮质类固醇治疗后才有所改善。基于该病例报告,讨论了关于Landry-Guillain-Barre-Strohl综合征发病机制和治疗的基本考虑因素。