Roberts P F, Venuta F, Rendina E, De Giacomo T, Coloni G F, Follette D M, Richman D P, Benfield J R
Division of Cardiothoracic Surgery, University of California, Davis, Sacramento 95817, Calif, USA.
J Thorac Cardiovasc Surg. 2001 Sep;122(3):562-8. doi: 10.1067/mtc.2001.116191.
Thymectomy is an effective and accepted treatment for myasthenia gravis, but thymectomy for ocular myasthenia gravis (Osserman stage I) is controversial.
To assess the efficacy and propriety of thymectomy for the treatment of ocular myasthenia gravis.
We conducted a review and follow-up of all patients who had thymectomy for the treatment of ocular myasthenia gravis between 1970 and 1998 at the University of California, Davis, Medical Center, and the University of Rome, "La Sapienza," Rome, Italy. Patient response to thymectomy was categorized as follows: cured, patients who became symptom-free and required no further medication; improved, patients who required less medication and whose symptoms were less severe; unchanged, patients whose symptoms and medications were the same; worse, patients who had more severe symptoms, needed more medication, or died.
Sixty-one patients (mean age 37 years; range 14-73 years) were followed up for a mean duration of 9 years (range 0.5-29 years). Ocular myasthenia gravis with mixed and cortical thymomas, stages I to IV, occurred in 12 patients, and ocular myasthenia without thymomas occurred in 49 patients. Transsternal thymectomy (n = 55) and transcervical thymectomy (n = 6) resulted in cure in 31 (51%) patients, improvement in 12 (20%) patients, no change in 16 (26%) patients, and worsening of symptoms (including 1 postoperative death) in 2 patients. Patient outcomes were statistically independent of the duration of preoperative symptoms (mean 9.5 months), patient age, or the presence or absence of thymoma. In patients with ocular myasthenia, 70% were cured or improved after thymectomy; in the subgroup of patients with ocular myasthenia and thymoma, 67% were cured or improved.
Thymectomy is an effective and safe treatment for patients with ocular myasthenia gravis.
胸腺切除术是治疗重症肌无力的一种有效且被认可的方法,但对于眼肌型重症肌无力(Osserman Ⅰ期)进行胸腺切除术存在争议。
评估胸腺切除术治疗眼肌型重症肌无力的疗效和合理性。
我们对1970年至1998年间在加利福尼亚大学戴维斯分校医学中心以及意大利罗马“La Sapienza”大学因治疗眼肌型重症肌无力而接受胸腺切除术的所有患者进行了回顾和随访。患者对胸腺切除术的反应分类如下:治愈,即症状消失且无需进一步药物治疗的患者;改善,即所需药物减少且症状减轻的患者;无变化,即症状和药物治疗情况相同的患者;恶化,即症状更严重、需要更多药物治疗或死亡的患者。
61例患者(平均年龄37岁;范围14 - 73岁)平均随访9年(范围0.5 - 29年)。12例患者为伴有混合性和皮质型胸腺瘤的眼肌型重症肌无力,Ⅰ至Ⅳ期,49例患者为无胸腺瘤的眼肌型重症肌无力。经胸骨胸腺切除术(n = 55)和经颈部胸腺切除术(n = 6)使31例(51%)患者治愈,12例(20%)患者改善,16例(26%)患者无变化,2例患者症状恶化(包括1例术后死亡)。患者的预后在统计学上与术前症状持续时间(平均9.5个月)、患者年龄或胸腺瘤的有无无关。在眼肌型重症肌无力患者中,70%在胸腺切除术后治愈或改善;在眼肌型重症肌无力合并胸腺瘤的亚组患者中,67%治愈或改善。
胸腺切除术是治疗眼肌型重症肌无力患者的一种有效且安全的方法。