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早期妊娠失败患者的核型与超声检查结果之间的相关性

Correlation between karyotype and ultrasound findings in patients with failed early pregnancy.

作者信息

Goldstein S R, Kerenyi T, Scher J, Papp C

机构信息

New York University School of Medicine, NY, USA.

出版信息

Ultrasound Obstet Gynecol. 1996 Nov;8(5):314-7. doi: 10.1046/j.1469-0705.1996.08050314.x.

Abstract

The aim of this retrospetive study was to identify any consistent patterns between ultrasound findings in failed pregnancies and either normal or abnormal karyotypes. The study involved 102 women in whom the diagnosis of early pregnancy failure was made sonographically. The criteria for a failed pregnancy were: a gestational sac with a mean diameter of > 12 mm without a yolk sac; a yolk sac of > 6 mm mean diameter with or without abnormal morphology that ultimately failed to develop an embryonic structure; and an embryo with a crown--rump length (CRL) of > 5 mm without cardiac activity, or the loss of previously identified cardiac activity. All patients underwent elective dilatation and curettage (D & C) and products of conception were sent for karyotyping. Forty-four pregnancies (43%) had abnormal karyotypes. Of these, 33 (75%) were trisomies. The other 11 included four triploidies, one tetraploidy, two with monosomy X, and four others (unbalanced complement, isochromosome, terminal deletion and translocation). Fifty-eight pregnancies (57%) had normal karyotypes, of which 52 were 46,XX and six were 46,XY. The furthest sonographic anatomic landmark achieved did not differ with respect to karyotypic findings. An abnormal yolk sac was found in 10/58 cases (17.2%) with normal karyotypes and 8/44 cases (18.2%) with abnormal karyotypes. There were eight cases of trisomy 16, of which only two manifested an embryonic structure, but neither of which had cardiac activity; the largest was 4 mm. There were four cases of trisomy 22, of which three developed embryos with a CRL of > 10 mm with cardiac activity (11, 11 and 18 mm, respectively). In three cases of mosaicism, embryos developed cardiac activity, and were 9, 19 and 16 mm. Two cases of monosomy X had embryos of 14 and 24 mm. Only one out of five cases with multiple trisomies developed to a point at which any embryonic structure was identifiable on ultrasound examination. The ultrasound appearance of early pregnancy failure in terms of furthest anatomic landmark reached was not significantly different in cases with normal or abnormal karyotype. An abnormally enlarged yolk sac, presumably secondary to hydropic change, is a non-specific finding of failed pregnancy, and did not correlate with karyotypic abnormality (trisomy 22, mosaic, monosomy X) seem to develop further prior to embryonic demise than those with certain others (trisomy 16, multiple trisomies and unusual other variants.

摘要

这项回顾性研究的目的是确定妊娠失败时超声检查结果与正常或异常核型之间是否存在一致的模式。该研究纳入了102例经超声诊断为早期妊娠失败的女性。妊娠失败的标准为:平均直径>12 mm的妊娠囊且无卵黄囊;平均直径>6 mm的卵黄囊,无论形态是否异常,最终均未发育出胚胎结构;头臀长(CRL)>5 mm的胚胎且无心脏活动,或先前已确定的心脏活动消失。所有患者均接受了选择性刮宫术(D&C),并将妊娠产物送去进行核型分析。44例妊娠(43%)核型异常。其中,33例(75%)为三体。另外11例包括4例三倍体、1例四倍体、2例X单体,以及其他4例(染色体不平衡、等臂染色体、末端缺失和易位)。58例妊娠(57%)核型正常,其中52例为46,XX,6例为46,XY。超声检查所达到的最远解剖标志在核型结果方面并无差异。在58例核型正常的病例中有10例(17.2%)发现卵黄囊异常,在44例核型异常的病例中有8例(18.2%)发现卵黄囊异常。有8例三体16,其中只有2例表现出胚胎结构,但均无心脏活动;最大的为4 mm。有4例三体22,其中3例发育出CRL>10 mm且有心脏活动的胚胎(分别为11、11和18 mm)。在3例嵌合体病例中,胚胎发育出心脏活动,分别为9、19和16 mm。2例X单体病例中的胚胎分别为14和24 mm。在5例多重三体病例中,只有1例发育到超声检查可识别任何胚胎结构的阶段。就超声检查所达到的最远解剖标志而言,核型正常或异常的妊娠失败病例的超声表现无显著差异。异常增大的卵黄囊,推测继发于水肿改变,是妊娠失败的非特异性表现,且与核型异常无关(三体22、嵌合体、X单体)在胚胎死亡前似乎比某些其他情况(三体16、多重三体和其他异常变体)发育得更远。

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