Jakobi P, Weiner Z, Best L, Itskovitz-Eldor J
Department of Obstetrics and Gynecology, Rambam Medical Center, Haifa 31096, Israel.
Obstet Gynecol. 2001 May;97(5 Pt 2):813-4. doi: 10.1016/s0029-7844(00)01091-7.
Most congenital pulmonary arteriovenous malformations are associated with hereditary hemorrhagic telangiectasia. During pregnancy, pulmonary hemorrhage can occur, compromising maternal and fetal health.
We studied three pregnancies in two women with hemorrhagic telangiectasia complicated by pulmonary arteriovenous malformations. A 28-year-old primigravida's fetus died at 25 weeks' gestation, and she had embolotherapy with coil springs, which corrected the hypoxemic state. In a subsequent pregnancy she delivered a healthy 2315-g infant at 38 weeks' gestation. A 19-year-old primigravida had spontaneous hemothorax at 26 weeks' gestation with severe hypoxemia and a growth-restricted fetus without umbilical artery diastolic flow. Pulmonary arteriovenous malformation was diagnosed by computed tomography of the maternal lung. She had continued pulmonary bleeding, so emergency lung lobectomy was done. Maternal hypoxemia and umbilical diastolic flow improved, and she had term delivery of a healthy 2250-g infant.
Antenatal diagnosis and treatment of women with hereditary hemorrhagic telangectasia and pulmonary arteriovenous malformations might prevent potentially life-threatening fetomaternal complications.
大多数先天性肺动静脉畸形与遗传性出血性毛细血管扩张症相关。孕期可发生肺出血,危及母婴健康。
我们研究了两名患有出血性毛细血管扩张症并合并肺动静脉畸形的女性的三次妊娠情况。一名28岁初产妇的胎儿在妊娠25周时死亡,她接受了弹簧圈栓塞治疗,纠正了低氧状态。在随后的一次妊娠中,她在妊娠38周时产下一名体重2315克的健康婴儿。一名19岁初产妇在妊娠26周时出现自发性血胸,伴有严重低氧血症和胎儿生长受限且脐动脉舒张期血流消失。通过对产妇肺部进行计算机断层扫描诊断为肺动静脉畸形。她持续肺出血,因此进行了急诊肺叶切除术。产妇低氧血症和脐动脉舒张期血流情况改善,她足月产下一名体重2250克的健康婴儿。
对患有遗传性出血性毛细血管扩张症和肺动静脉畸形的女性进行产前诊断和治疗可能预防潜在的危及生命的母婴并发症。