Botez M I, Peyronnard J M, Bachevalier J, Charron L
Arch Neurol. 1978 Sep;35(9):581-4. doi: 10.1001/archneur.1978.00500330029005.
We studied five patients (two men and three women, age between 58 and 76 years) with clinical and electrophysiological signs of polyneuropathy. Routine neurological, hematological, and gastroenterological studies as well as procedures to test fat malabsorption were performed. Folate determinations were done using both radioactive and Lactobacillus casei methods. Two patients displayed the signs of subacute combined degeneration of the spinal cord with polyneuropathy, while three had only signs of neuropathy. All had low serum folate concentration, long-standing gastrointestinal disease, and deficient folate intake. The D-xylose absorption test gave values in all patients, while none displayed the classical malabsorption syndrome. The patients had substantial improvement or recovered (according to clinical and electrophysiological measurements) after periods ranging from 9 to 39 months of folate therapy. Such acquired folate-responsive polyneuropathy has two principal characteristics: mixed sensorimotor with mainly sensory deficits, and involvement of one or both of the lower extremities much more extensively than the upper extremities.
我们研究了5例患有多发性神经病临床和电生理体征的患者(2名男性和3名女性,年龄在58至76岁之间)。进行了常规神经学、血液学和胃肠病学检查以及检测脂肪吸收不良的程序。采用放射性和干酪乳杆菌法进行叶酸测定。2例患者表现出脊髓亚急性联合变性伴多发性神经病的体征,而3例仅表现出神经病体征。所有患者血清叶酸浓度均较低,患有长期胃肠疾病且叶酸摄入不足。所有患者的D-木糖吸收试验结果均正常,无一例表现出典型的吸收不良综合征。在接受9至39个月的叶酸治疗后,患者(根据临床和电生理测量)有显著改善或康复。这种获得性叶酸反应性多发性神经病有两个主要特征:感觉运动混合性,主要为感觉缺陷,以及一个或双下肢受累比上肢广泛得多。