Fait G, Daniel Y, Kupferminc M J, Gull I, Peyser M R, Lessing J B
Department of Obstetrics and Gynecology A, Serlin Maternity Hospital, Tel Aviv Sourasky Medical Center, Israel.
Hum Reprod. 1996 Nov;11(11):2544-5. doi: 10.1093/oxfordjournals.humrep.a019156.
Klippel-Trénaunay-Weber syndrome is a rare congenital deep-vein malformation. Pregnancy in patients with this syndrome is rare and only a few cases have been reported. Known obstetrical risks in pregnant patients with this syndrome include bleeding from angiomata in the genitalia, and coagulation disturbances. We present a 31 year old woman with this syndrome who, on two occasions, delivered small-for-gestational-age neonates. This may have been due to placental insufficiency caused by angiomatosis related to the syndrome.
克-特-韦综合征是一种罕见的先天性深部静脉畸形。患有这种综合征的患者怀孕很罕见，仅有少数病例报道。患有这种综合征的孕妇已知的产科风险包括生殖器血管瘤出血和凝血功能障碍。我们报告了一名患有这种综合征的31岁女性，她曾两次分娩出小于孕周的新生儿。这可能是由于与该综合征相关的血管瘤病导致的胎盘功能不全。
