Hereditary hemorrhagic telangiectasia with pulmonary arteriovenous malformations

被引:15
|
作者
Jakobi, P [1 ]
Weiner, Z
Best, L
Itskovitz-Eldor, J
机构
[1] Rambam Med Ctr, Dept Obstet & Gynecol, IL-31096 Haifa, Israel
[2] Rambam Med Ctr, Dept Thorac Surg, IL-31096 Haifa, Israel
来源
OBSTETRICS AND GYNECOLOGY | 2001年 / 97卷 / 05期
关键词
D O I
10.1016/S0029-7844(00)01091-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Most congenital pulmonary arteriovenous malformations are associated with hereditary hemorrhagic telangiectasia. During pregnancy, pulmonary hemorrhage can occur, compromising maternal and fetal health. Cases: 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 now. 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. Conclusion: Antenatal diagnosis and treatment of women with hereditary hemorrhagic telangectasia and pulmonary arteriovenous malformations might prevent potentially life-threatening fetomaternal complications. (C) 2001 by The American College of Obstetricians and Gynecologists.
引用
收藏
页码:813 / 814
页数:2
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