Dalakas M C
Eur Neurol. 1986;25(5):381-7. doi: 10.1159/000116038.
Fourteen survivors of paralytic poliomyelitis experienced new symptoms after years of stability. Seven patients had lost functional capacity, with joint pain, instability and recurrent falls, but were again stable and remained essentially unchanged during a 3-year follow-up period. Seven others had late postpoliomyelitis muscular atrophy (PPMA) with new weakness, wasting, fasciculations and myalgia in muscles originally spared or seemingly recovered. Muscle biopsy from newly affected muscles showed new and chronic denervation with interstitial inflammation in 3 patients. Antibody titers to poliomyelitis virus were not elevated in the CSF, but oligoclonal IgG bands were found in 3 PPMA patients. During the 3-year follow-up period, PPMA patients showed signs of slow progression which continued to be focal. It is concluded that the new symptoms in postpolio patients may be musculoskeletal and relatively stable, or due to a slowly progressive, focal, and apparent benign new motor neuron deterioration.
14名麻痹性脊髓灰质炎幸存者在病情稳定多年后出现了新症状。7名患者出现功能丧失,伴有关节疼痛、不稳定和反复跌倒,但再次稳定下来,并且在3年随访期内基本保持不变。另外7名患者患有迟发性脊髓灰质炎后肌肉萎缩(PPMA),原本未受累或看似已恢复的肌肉出现新的无力、消瘦、肌束震颤和肌痛。对新受累肌肉进行的肌肉活检显示,3例患者出现新的和慢性去神经支配以及间质炎症。脑脊液中脊髓灰质炎病毒抗体滴度未升高,但在3例PPMA患者中发现寡克隆IgG带。在3年随访期内,PPMA患者表现出缓慢进展的迹象,且仍为局灶性。结论是,脊髓灰质炎后遗症患者的新症状可能是肌肉骨骼方面的且相对稳定,或者是由于缓慢进展的、局灶性的、明显良性的新运动神经元退化所致。