Mahony B S, Nyberg D A, Hirsch J H, Petty C N, Hendricks S K, Mack L A
Division of Ultrasound, Swedish Hospital Medical Center, Seattle, WA 98104.
Radiology. 1988 Dec;169(3):715-21. doi: 10.1148/radiology.169.3.3055035.
The authors prospectively studied 20 fetuses with mild dilatation of the lateral cerebral ventricles but no other detectable central nervous system abnormality. One case (5%) occurred in a diabetic pregnancy, and three (15%) involved twin pregnancies. Fifteen (75%) fetuses were male, and one (5%) had trisomy 21. Postnatal follow-up at 15-31 months showed a normal outcome in eight cases (40%), an uncertain prognosis in four cases (20%), and death in eight cases (40%). Serial antenatal sonograms were obtained in 17 cases. Among the eight cases with a normal outcome, seven demonstrated no additional sonographic abnormalities and six showed resolution of the ventricular dilatation antenatally. Conversely, all 12 fetuses with demise or an uncertain prognosis demonstrated additional sonographic abnormalities, and six showed stable or progressive ventricular dilatation on follow-up sonograms. Since mild idiopathic lateral ventricular dilatation has a widely variable prognosis, antenatal detection of this finding warrants search for additional findings and follow-up sonography.
作者前瞻性地研究了20例侧脑室轻度扩张但无其他可检测到的中枢神经系统异常的胎儿。其中1例(5%)发生于糖尿病妊娠,3例(15%)为双胎妊娠。15例(75%)胎儿为男性,1例(5%)患有21三体综合征。15至31个月的产后随访显示,8例(40%)预后正常,4例(20%)预后不确定,8例(40%)死亡。17例进行了系列产前超声检查。在8例预后正常的病例中,7例未发现其他超声异常,6例产前脑室扩张消失。相反,所有12例死亡或预后不确定的胎儿均发现其他超声异常,6例随访超声显示脑室扩张稳定或进展。由于轻度特发性侧脑室扩张的预后差异很大,产前发现这一情况需要寻找其他发现并进行随访超声检查。