摘要
报告40例胸腺肿瘤合并重症肌无力(MG)的手术治疗效果。本组包括完全切除肿瘤和胸腺26例,次全切除肿瘤10例,组织活检4例。结果手术死亡1例(2.5%),术后1年内死亡8例(20.5%)。31例术后随访3~12年,5年生存率为61.3%,10年生存率27.7%;其中非浸润型胸腺瘤分别为76.9%和30.0%,浸润型胸腺瘤则为50.0%和25.0%。MG术后缓解改善率为80.6%,术后肌无力危象发生率为40.0%,抢救成功率为93.8%,结论显示手术治疗胸腺肿瘤合并MG,如严格掌握手术指征,可获得较好的疗效和预后。
Aim:To evaluate the outcome of surgical treatment for myasthenia gravis. Clinical material and method:Forty patients with thymoma associated with myasthenia gravis were treated surgically.There were 26 males and 14 females with a mean age of 44.2 years.According to Osserman classification,stage IIa was in 6 patients,stage IIb in 14,stage III in 5 and stage IV in 15 patients.Surgical procedures included complete thymectomy in 26 patients,partial thymectomy in 10 and simple biopsy in 4 patients.Result:There was one operative death with a hospital mortality rate of 2.5%.The cause of death was respiratory insufficiency.Late death occurred in 8 patients.Overall five and tenyear survival rates were 61.3% and 27.7%,respectively.The 5 and 10year survival rates were 76.9% and 30.0% for noninfiltrated tumor and 50.0% and 25.0% for infiltrated tumor.40.0% of patients had complication of respiratory insufficiency after surgery.Complete improvement was achieved in 15 patients (48.4%),partial improvement in 10,no improvement in 4 and worse in 2. Conclusion:Thymectomy is the treatment of choice for thymoma with generalized myasthenia gravis.The operation offers a satisfactory percentage of clinical improvement with low mortality and morbidity rates.The surgical outcome is related to clinical staging of myasthenia gravis and perioperative management.
出处
《中华胸心血管外科杂志》
CSCD
北大核心
1998年第1期24-25,共2页
Chinese Journal of Thoracic and Cardiovascular Surgery