Berman A T, Tom L
Clin Orthop Relat Res. 1976 May(116):61-5.
Eleven cases of Guillain-Barre Syndrome in children between 1955 and 1973 demonstrate clinical course and residual permanent motor deficits. The rate of recovery from muscle paralysis and the long-term permanent muscle loss, and the resultant paralytic deficits may require treatment: tendon transfers, opponensplasties, spinal fusions, and Lambrinudi operations. The late permanent motor paralysis and residual joint deformities secondary to GBS in children has a higher incidence and severity than in adults, and an intensive rehabilitation program in imperative. Frequent, extended follow-up, and muscle testing records are absolutely essential in children.
1955年至1973年间11例儿童吉兰-巴雷综合征病例展示了临床病程及残留的永久性运动功能缺损。肌肉麻痹的恢复率、长期永久性肌肉丧失以及由此导致的麻痹性缺损可能需要进行治疗:肌腱转移术、对掌肌成形术、脊柱融合术和兰布里努迪手术。儿童吉兰-巴雷综合征继发的晚期永久性运动麻痹和残留关节畸形的发生率和严重程度高于成人,因此必须进行强化康复计划。对儿童而言,频繁、长期的随访以及肌肉测试记录绝对至关重要。