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胎儿脉络丛囊肿:良性解剖变异还是病理实体?41例报告并文献复习

Choroid plexus cysts in the fetus: a benign anatomic variant or pathologic entity? Report of 41 cases and review of the literature.

作者信息

Chitkara U, Cogswell C, Norton K, Wilkins I A, Mehalek K, Berkowitz R L

机构信息

Department of Obstetrics, Gynecology, and Reproductive Science, Mount Siani School of Medicine, New York, New York.

出版信息

Obstet Gynecol. 1988 Aug;72(2):185-9.

PMID:3292976
Abstract

During a 22-month period, 6288 women undergoing prenatal sonographic studies in the second and third trimesters were evaluated prospectively to determine the incidence of choroid plexus cysts in the fetus, to follow the natural course of these cysts in intrauterine life, and to determine the association of chromosomal and anatomic anomalies in these fetuses. We diagnosed choroid plexus cysts in 41 fetuses, an incidence of 0.65%. Unilateral and bilateral cysts were equally frequent, and in most cases diagnosed by 21 weeks' gestation. On follow-up scans, the cysts had completely disappeared by 23-24 weeks in 80% of the cases, and by 28 weeks in another 10%. Once resolved, the cysts did not recur, and a normal sonogram in the late second trimester predicted normal scans in late pregnancy and in the neonate. One fetus had a chromosomal abnormality (trisomy 18). Associated anatomic anomalies were detected in three fetuses, including the one with trisomy 18. We believe that in the great majority of cases, fetal choroid plexus cysts are benign transient variants of normal intracranial anatomy. It is, however, important to conduct a careful sonographic search for associated anomalies. Chromosomal studies are strongly recommended whenever associated anatomic abnormalities are detected and when the choroid plexus cysts are large, bilateral, and persistent beyond 20-22 weeks' gestation.

摘要

在22个月的时间里,对6288名在孕中期和孕晚期接受产前超声检查的妇女进行了前瞻性评估,以确定胎儿脉络丛囊肿的发生率,追踪这些囊肿在宫内的自然发展过程,并确定这些胎儿中染色体和解剖结构异常之间的关联。我们在41例胎儿中诊断出脉络丛囊肿,发生率为0.65%。单侧和双侧囊肿的发生频率相同,大多数病例在妊娠21周时被诊断出来。在后续扫描中,80%的病例中囊肿在23 - 24周时完全消失,另有10%在28周时消失。一旦囊肿消失,就不会复发,孕中期晚期的正常超声检查结果预示着妊娠晚期和新生儿期的扫描结果也正常。有1例胎儿存在染色体异常(18三体)。在3例胎儿中检测到相关的解剖结构异常,包括那例18三体的胎儿。我们认为,在绝大多数情况下,胎儿脉络丛囊肿是正常颅内解剖结构的良性短暂变异。然而,仔细进行超声检查以寻找相关异常情况很重要。当检测到相关解剖结构异常以及脉络丛囊肿较大、双侧且在妊娠20 - 22周后仍持续存在时,强烈建议进行染色体检查。

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