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格林—巴利综合征的予后一般良好,急性期存活者通常于起病后数周开始恢复,但长期残废的未成年病人自然恢复的可能性很小。本文报告2例严重残废6及12个月的患儿用多不饱和脂酸(P.U.F.A.)饮食治愈。两例均为女孩,年龄4及6岁,因患格林—巴利综合征引起严重的四肢肌无力,腱反射对称性减弱或消失,应用强的松龙(1例加用环磷酰胺)治疗无效而采用P.U.F.A.饮食治疗。P.U.F.A.饮食是治疗高胆固醇血症的标准低脂饮食(无奶油、干酪及含脂肪的肉,只有脱脂乳。)加葵花子油10毫升,3次/日,例1再加麦胚油0.5毫升,3次/日。
Guillain-Barré syndrome is generally favored, with acute-phase survivors usually recovering weeks after onset, but there is very little chance of spontaneous recovery of long-term disabled children. This article reports two cases of severe disability 6 and 12 months of children with polyunsaturated fatty acid (P.U.F.A.) diet cure. Both were girls, aged 4 and 6 years old. Severe limb muscle weakness caused by Guillain-Barre syndrome, symmetry of tendon reflexes diminished or disappeared, and treatment with prednisolone (1 plus cyclophosphamide) Invalid and PUFA diet treatment. The PUFA diet is a standard, low-fat diet for the treatment of hypercholesterolemia (cream-free, cheeses and fat-containing meat, skim milk only.) Plus sunflower oil 10ml, 3 times daily, Example 1 plus wheat germ oil 0.5ml, 3 times / day.