Kyle R A, Greipp P R
Mayo Clin Proc. 1983 Oct;58(10):665-83.
At the Mayo Clinic from 1970 to 1980, 229 patients with primary systemic amyloidosis (AL) were examined. Nephrotic syndrome, congestive heart failure, orthostatic hypotension, carpal tunnel syndrome, and peripheral neuropathy were often associated features. Electrophoresis of the serum revealed a spike in only 40%, but immunoelectrophoresis disclosed a monoclonal protein in 68%. Eighty-nine percent of patients in whom it was sought had a monoclonal protein in the serum or urine. The diagnosis of amyloidosis was made before death in 96% of the patients. The preferred sites for biopsy were the bone marrow, rectum, kidney, carpal ligament, liver, small intestine, skin, and sural nerve. The median survival of the 229 patients was 12 months. The median survival of the 77 patients with congestive heart failure was 6 months after the onset of symptoms. Congestive heart failure or arrhythmias accounted for death in 40%. Treatment for amyloidosis is unsatisfactory but includes melphalan, prednisone, colchicine, and dimethyl sulfoxide.
1970年至1980年期间,梅奥诊所对229例原发性系统性淀粉样变(AL)患者进行了检查。肾病综合征、充血性心力衰竭、体位性低血压、腕管综合征和周围神经病变是常见的相关特征。血清电泳仅在40%的患者中显示有峰,但免疫电泳显示68%的患者存在单克隆蛋白。在进行检测的患者中,89%的患者血清或尿液中有单克隆蛋白。96%的患者在死亡前确诊为淀粉样变。活检的首选部位是骨髓、直肠、肾脏、腕韧带、肝脏、小肠、皮肤和腓肠神经。229例患者的中位生存期为12个月。77例充血性心力衰竭患者症状出现后的中位生存期为6个月。充血性心力衰竭或心律失常导致40%的患者死亡。淀粉样变的治疗效果不理想,但包括美法仑、泼尼松、秋水仙碱和二甲亚砜。