Tabor A, Bang J, Philip J
Prenat Diagn. 1981 Oct;1(4):281-3. doi: 10.1002/pd.1970010408.
We report three cases of Turner's syndrome with cystic hygromata, which were diagnosed by routine ultrasound scanning before amniocentesis in the second trimester of pregnancy. Maternal and amniotic level of alpha-fetoprotein were normal. Karyotyping carried out afterwards showed a 45,X karyotype. Our data indicate, that cystic hygromata in Turner's syndrome may coexist with a normal amniotic fluid AFP, thus questioning the theory of leakage from the hygroma. It remains to be investigated if all cases of Turner's syndrome present a cystic hygroma in utero.
我们报告了3例患有囊状水瘤的特纳综合征病例,这些病例在妊娠中期羊膜穿刺术前通过常规超声扫描得以诊断。母血和羊水甲胎蛋白水平均正常。随后进行的染色体核型分析显示为45,X核型。我们的数据表明,特纳综合征中的囊状水瘤可能与羊水甲胎蛋白正常并存,从而对水瘤渗漏理论提出质疑。对于所有特纳综合征病例在子宫内是否都存在囊状水瘤仍有待研究。