Carr S R, Gilchrist J M, Abuelo D N, Clark D
Department of Obstetrics and Gynecology, Women and Infants' Hospital of Rhode Island, Providence.
Obstet Gynecol. 1991 Sep;78(3 Pt 2):485-9.
Maternal myasthenia gravis has been associated with the presence of neonatal myasthenia and sometimes fatal congenital anomalies. As a result, antenatal therapy directed at fetal sequelae may be indicated. We present the case of a pregnant myasthenic woman whose two previous pregnancies had ended in neonatal deaths from fetal deformations that were presumably due to maternal myasthenia. Serial plasmaphereses and oral prednisone therapy were used in an attempt to depress maternal anti-acetylcholine receptor antibody titers. As anti-acetylcholine receptor antibody titers fell, fetal breathing movements became apparent by ultrasound, and as these titers rose, no fetal breathing movements were apparent. Our patient delivered an infant with transient neonatal myasthenia but normal pulmonary development and no deformations. We suggest that the therapy given may have improved the outcome of this pregnancy compared with her two previous pregnancies.
重症肌无力母亲与新生儿肌无力的出现以及有时致命的先天性异常有关。因此,针对胎儿后遗症的产前治疗可能是必要的。我们报告一例重症肌无力孕妇病例,她之前的两次妊娠均以胎儿畸形导致的新生儿死亡告终,推测胎儿畸形是由母亲的重症肌无力引起的。为降低母亲抗乙酰胆碱受体抗体滴度,采用了连续血浆置换和口服泼尼松治疗。随着抗乙酰胆碱受体抗体滴度下降,超声检查可明显观察到胎儿呼吸运动;而当这些滴度上升时,则未见明显的胎儿呼吸运动。我们的患者分娩出一名患有短暂性新生儿肌无力但肺部发育正常且无畸形的婴儿。我们认为,与她之前的两次妊娠相比,此次给予的治疗可能改善了本次妊娠的结局。