, Ulm, Germany.
Prenatal Medicine & Genetics, praenatal.de, Düsseldorf, Germany.
Arch Gynecol Obstet. 2022 Oct;306(4):1037-1044. doi: 10.1007/s00404-021-06394-z. Epub 2022 Jan 11.
A short fetal femur in prenatal diagnosis might be an indicator for intrauterine growth retardation (IUGR), a genetically determined small child (SGA) with or without associated fetal malformations and/or an adverse fetal outcome.
1373 singleton pregnancies with a femoral length < 5th percentile detected between 1999 and 2015 during second-trimester screening in a tertiary prenatal diagnostic center were subjected to a descriptive retrospective analysis with regard to fetal characteristics as well as pregnancy outcome.
685 (49.9%) fetuses presented an isolated short femur, while 688 (50.1%) showed additional abnormalities. 293 (42.6%) of those were SGA babies without any malformation, while 395 (57.4%) had one or more severe anomaly of the following organ systems: 157 (11.5%) cardiovascular, 101 (7.4%) musculoskeletal, 82 (6.0%) urogenital, 72 (5.2%) cerebrocephalic, 50 (3.6%) gastrointestinal, and 5 (0.4%) thoracic. 75 (5.5%) of the fetuses showed chromosomal aberrations of which Trisomy 13, 18 and 21 were found in 2, 13 and 27 of the cases, respectively. Fetuses with associated malformations had a significantly lower live birth rate than those without (64.2% vs. 98.1%, p < 0.001); in addition, a higher rate of preterm births 36.6% vs. 11.3%, p < 0.001) and SGA babies (51.4% vs. 30.4%, p < 0.001) were observed in the first collective.
Diagnosis of a short fetal femur should lead to an extended organ screening; in the case of associated abnormalities, additional genetic testing has to be offered, as well as intensified pregnancy monitoring in pregnancies at risk for IUGR and/or preterm birth.
产前诊断中胎儿股骨过短可能是宫内生长受限(IUGR)的一个指标,这是一种由遗传决定的小胎儿(SGA),伴有或不伴有胎儿畸形和/或不良的胎儿结局。
在一家三级产前诊断中心,对 1999 年至 2015 年期间在中期妊娠筛查中检测到的 1373 例股骨长度<第 5 百分位数的单胎妊娠进行描述性回顾性分析,分析胎儿特征和妊娠结局。
685 例(49.9%)胎儿存在单纯股骨过短,688 例(50.1%)存在其他异常。其中 293 例(42.6%)为无畸形的 SGA 婴儿,395 例(57.4%)存在以下一个或多个严重畸形的器官系统:心血管 157 例(11.5%)、肌肉骨骼 101 例(7.4%)、泌尿生殖 82 例(6.0%)、颅脑 72 例(5.2%)、胃肠道 50 例(3.6%)和胸 5 例(0.4%)。75 例(5.5%)胎儿存在染色体异常,其中 2 例为三体 13、18 和 21,13 和 27 例分别为 13 和 27。伴有畸形的胎儿活产率明显低于无畸形的胎儿(64.2% vs. 98.1%,p<0.001);此外,第一组中早产率(36.6% vs. 11.3%,p<0.001)和 SGA 婴儿(51.4% vs. 30.4%,p<0.001)的发生率也较高。
胎儿股骨过短的诊断应导致进行广泛的器官筛查;在存在畸形的情况下,必须提供额外的基因检测,并对 IUGR 和/或早产风险的妊娠进行强化妊娠监测。