Okada F, Yamashita I, Suwa N
Arch Neurol. 1975 Mar;32(3):146-51. doi: 10.1001/archneur.1975.00490450026002.
Two men had acute nonprogressive pandysautonomia. Both of them showed orthostatic hypotension, fainting in upright position, pupillary disturbances, diminished sweating, anacidity, and impotence. Case 1 showed considerable but inadequate improvement within 31 months. Case 2 recovered completely after 11 months. Clinical and pharmacodynamic investigations suggested that the main lesion was located in postganglionic fibers in case 1 and in preganglionic fibers in case 2. The cause of this disorder is unknown, although both patients had undergone substantial weight loss.
两名男性患有急性非进行性全自主神经功能不全。他们均表现为直立性低血压、直立位晕厥、瞳孔功能障碍、出汗减少、胃酸缺乏和阳痿。病例1在31个月内有显著但不完全的改善。病例2在11个月后完全康复。临床和药效学研究表明,病例1的主要病变位于节后纤维,病例2的主要病变位于节前纤维。尽管两名患者均有明显体重减轻,但这种疾病的病因尚不清楚。