Katz S G, Nelson I W, Atkins R M, Duthie R B
Department of Orthopaedic Surgery, Nuffield Orthopaedic Centre, Headington, Oxford, England.
J Bone Joint Surg Am. 1991 Aug;73(7):1016-9.
Between 1962 and 1986, eighty-one of the 1351 admissions of patients who had hemophilia to the Nuffield Orthopaedic Centre were for peripheral nerve lesions. Eighty-eight such lesions were identified in fifty-four patients, and thirty-nine of these patients (sixty-one lesions) had adequate follow-up (mean, 8.4 years; range, four months to eighteen years). The femoral nerve was most commonly involved, but involvement of other peripheral nerves also occurred. In thirty (49 per cent) of the sixty-one lesions, the nerve had full motor and sensory recovery; in twenty-one (34 per cent), a residual sensory deficit; and in ten (16 per cent), both a persistent motor and sensory deficit. Patients who had antibodies to factor VIII were significantly less likely to recover full motor or sensory function than were those who did not have such antibodies, and the time to full motor recovery in these patients was significantly longer.
1962年至1986年间,在纳菲尔德骨科中心收治的1351例血友病患者中,有81例是因周围神经病变入院。在54例患者中发现了88处此类病变,其中39例患者(61处病变)获得了充分的随访(平均8.4年;范围为4个月至18年)。股神经受累最为常见,但其他周围神经也会受累。在61处病变中的30处(49%),神经运动和感觉功能完全恢复;21处(34%)有残留感觉障碍;10处(16%)存在持续性运动和感觉障碍。与没有抗凝血因子VIII抗体的患者相比,有该抗体的患者完全恢复运动或感觉功能的可能性显著降低,且这些患者完全恢复运动功能的时间明显更长。