Massey J M, Sanders D B
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Muscle Nerve. 1993 May;16(5):458-60. doi: 10.1002/mus.880160504.
We report the use of single fiber electromyography (SFEMG) to demonstrate changes in the physiologic abnormality of myasthenia gravis (MG) during pregnancy. A 23-year-old became pregnant 15 months after the onset of mild ocular weakness. On initial evaluation, SFEMG jitter measurements demonstrated a slight abnormality of neuromuscular transmission. There was no change in severity of clinical disease or jitter measurements until the third trimester, when she improved. Jitter measurements at that time were normal. Labor was normal and she delivered a normal male. Three days postpartum, myasthenic weakness recurred temporarily and jitter measurements showed worsening. At 16 days and 6 weeks postpartum, she had only minimal medial rectus weakness and jitter studies were normal. Three months postpartum, ocular symptoms recurred and jitter measurements were slightly abnormal. She continued to worsen, developing limb muscle and severe ocular muscle weakness at 4 months postpartum. She was treated with plasma exchange and thymectomy. Prednisone was added 2 months after thymectomy due to continued worsening and development of oropharyngeal weakness. Three years postpartum she was taking prednisone 10 mg every other day and had only slight weakness of neck flexors, and jitter studies were again normal.
我们报告了使用单纤维肌电图(SFEMG)来证明重症肌无力(MG)在妊娠期间生理异常的变化。一名23岁女性在轻度眼肌无力发作15个月后怀孕。初次评估时,SFEMG抖动测量显示神经肌肉传递略有异常。直到妊娠晚期她病情改善之前,临床疾病严重程度和抖动测量均无变化。当时的抖动测量结果正常。分娩过程正常,她产下一名正常男婴。产后三天,重症肌无力性肌无力暂时复发,抖动测量显示病情恶化。产后16天和6周时,她仅存在轻微的内直肌肌无力,抖动研究结果正常。产后三个月,眼部症状复发,抖动测量略有异常。她的病情继续恶化,在产后4个月出现肢体肌肉和严重眼肌无力。她接受了血浆置换和胸腺切除术治疗。由于病情持续恶化以及口咽肌无力的发展,胸腺切除术后2个月加用了泼尼松。产后三年,她每隔一天服用10毫克泼尼松,仅颈部屈肌有轻微无力,抖动研究结果再次正常。