Leonardi M R, Wolfe H M, Lanouette J M, Landwehr J B, Johnson M P, Evans M I
Department of Obstetrics and Gynecology, Center for Fetal Diagnosis and Therapy, Hutzel Hospital/Wayne State University, Detroit, Mich, USA.
Fetal Diagn Ther. 1998 Jan-Feb;13(1):49-52. doi: 10.1159/000020802.
To assess the risk of aneuploidy in cases of isolated choroid plexus cysts (CPCs) and to compare the risk when associated with minor or major anomalies.
All fetuses with CPCs and known karyotype were identified. CPCs were categorized as 'isolated' or associated with minor or major sonographic anomalies. Preexisting risk factors for aneuploidy were compared between groups. The frequency of aneuploidy was compared between fetuses with isolated CPCs and those with CPCs associated with minor or major anomalies. Continuous and categorical variables were analyzed using one-way analysis of variance or chi-square as appropriate with p < 0.05 considered significant.
One hundred and forty-nine fetuses with CPCs diagnosed at a mean gestational age of 19 weeks were identified. No significant differences in the frequency of preexisting risk factors for aneuploidy were identified between groups. Eighteen of 149 (12%) fetuses with CPCs had other sonographic anomalies; in 10 they were minor, and 2 of the 10 had abnormal karyotypes. Four of 8 fetuses with major anomalies were aneuploid. All 131 fetuses with isolated CPCs had normal karyotypes, and all aneuploid fetuses had additional anomalies.
The overall rate of aneuploidy in patients with CPCs was 4% with no abnormal karyotypes among isolated CPCs. The presence of even minor sonographic abnormalities substantially increased the risk of aneuploidy. Isolated CPCs identified sonographically may not place the patient at risk of aneuploidy, but should prompt a diligent search for other minor or major anomalies. The finding of any other anomaly warrants consideration for karyotypic evaluation.
评估孤立性脉络丛囊肿(CPC)病例中染色体非整倍体的风险,并比较其与轻微或严重异常相关时的风险。
识别所有患有CPC且已知核型的胎儿。CPC被分类为“孤立性”或与轻微或严重超声异常相关。比较各组之间预先存在的非整倍体风险因素。比较孤立性CPC胎儿与伴有轻微或严重异常的CPC胎儿的非整倍体频率。连续变量和分类变量分别使用单因素方差分析或卡方检验进行分析,以p<0.05为有统计学意义。
共识别出149例诊断为CPC的胎儿,平均孕周为19周。各组之间预先存在的非整倍体风险因素频率无显著差异。149例患有CPC的胎儿中有18例(12%)有其他超声异常;其中10例为轻微异常,10例中有2例核型异常。8例有严重异常的胎儿中有4例为非整倍体。所有131例孤立性CPC胎儿核型均正常,所有非整倍体胎儿均有其他异常。
CPC患者的总体非整倍体率为4%,孤立性CPC中无核型异常。即使是轻微的超声异常也会显著增加非整倍体的风险。超声检查发现的孤立性CPC可能不会使患者面临非整倍体风险,但应促使仔细寻找其他轻微或严重异常。发现任何其他异常均需考虑进行核型评估。