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孕中期脉络丛囊肿与18三体综合征

Second trimester choroid plexus cysts and trisomy 18.

作者信息

Sahinoglu Z, Uludogan M, Sayar C, Turkover B, Toksoy G

机构信息

Department of Perinatology, Zeynep Kamil Women and Children Hospital, Uskudar, Istanbul, Turkey.

出版信息

Int J Gynaecol Obstet. 2004 Apr;85(1):24-9. doi: 10.1016/j.ijgo.2003.08.016.

Abstract

OBJECTIVES

In this study, the aims were to reveal the incidence of isolated choroid plexus cyst in our population, and to discuss the accuracy of distinguishing either an isolated or non-isolated choroid plexus cyst.

METHODS

The study population was consisted of 10594 pregnant women. The patients with choroid plexus cysts were classified into two groups: isolated and non-isolated. Detailed ultrasonographic examination and genetic counseling were performed and triple screening test was ordered. The incidence, sensitivity, specificity, false-positive rate and likelihood ratio of cases with isolated choroid plexus cyst for trisomy 18 were determined.

RESULTS

Choroid plexus cysts were identified in 109 patients (109/10594; 1.02%). In 102 patients isolated choroid plexus cysts, and in seven patients additional fetal anomalies supporting trisomy 18 were detected. Trisomy 18 was detected in four patients, and one of them had isolated choroid plexus cyst. The likelihood ratio in cases of isolated choroid plexus cysts for trisomy 18 was 9.51 (95% confidence interval, 0.2-41).

CONCLUSIONS

According to the study the individual risk for trisomy 18 in isolated choroid plexus cyst should be calculated by using the likelihood ratio. These data allows the physician to express the individual risk of trisomy 18 and permits more accurate genetic counseling.

摘要

目的

本研究旨在揭示我们人群中孤立性脉络丛囊肿的发生率,并探讨区分孤立性或非孤立性脉络丛囊肿的准确性。

方法

研究人群包括10594名孕妇。脉络丛囊肿患者分为两组:孤立性和非孤立性。进行了详细的超声检查和遗传咨询,并安排了三联筛查试验。确定了孤立性脉络丛囊肿病例对于18三体的发生率、敏感性、特异性、假阳性率和似然比。

结果

109名患者(109/10594;1.02%)被发现有脉络丛囊肿。102例患者为孤立性脉络丛囊肿,7例患者检测到支持18三体的其他胎儿异常。4例患者检测到18三体,其中1例有孤立性脉络丛囊肿。孤立性脉络丛囊肿病例对于18三体的似然比为9.51(95%置信区间,0.2 - 41)。

结论

根据本研究,孤立性脉络丛囊肿中18三体的个体风险应通过似然比来计算。这些数据使医生能够表达18三体的个体风险,并进行更准确的遗传咨询。

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