Solerte Laura
Department of Obstetrics and Gynaecology, Prenatal Diagnosis Unit, Niguarda Hospital, Milano, Italy.
J Matern Fetal Neonatal Med. 2006 Feb;19(2):109-12. doi: 10.1080/14767050400028840.
A rare dysmorphologic fetal anomaly at the 17th week of gestation was suspected during a second trimester routine scan for fetal and maternal screening data. First findings were significant for a severe abdominal wall defect, limb and foot compromised positions. Fetal biometry was appropriate in biparietal diameter and head circumference measurements; the long upper bones were normal both for length and development. The patient was referred to a prenatal unit to complete the sonographic diagnosis. Two- and three-dimensional sonographic investigations were performed and techniques were complementary for fetal maldevelopment specification. Limb-body wall complex with lumbosacral spine torsion and lower limbs with severely abnormal features were identified. With 2D color Doppler, a heart defect was confirmed and the umbilical cord was missing from the amniotic cavity. An invasive procedure by amniocentesis was made to ascertain alpha-fetoprotein levels and fetal karyotype. Following parental counseling, pregnancy was terminated and feto-pathological examination confirmed the sonographic diagnosis. The 17-week fetus affected by limb-body wall complex is reported herein; 2D and 3D scans of the fetus identified organ displacement due to a combination of very early events.
在孕中期进行胎儿和母体筛查数据的常规扫描时,怀疑妊娠第17周出现罕见的胎儿形态异常。首次检查结果显示存在严重的腹壁缺损、肢体和足部位置异常。胎儿双顶径和头围测量的生物测量值正常;上肢长骨长度和发育均正常。患者被转诊至产前科室以完善超声诊断。进行了二维和三维超声检查,这些技术对胎儿发育异常的明确具有互补作用。确定为肢体-体壁复合体,伴有腰骶椎扭转,下肢具有严重异常特征。通过二维彩色多普勒,确认存在心脏缺陷,羊膜腔内未见脐带。进行了羊膜腔穿刺侵入性操作以确定甲胎蛋白水平和胎儿核型。在向父母咨询后,终止了妊娠,胎儿病理检查证实了超声诊断。本文报告了一名受肢体-体壁复合体影响的17周胎儿;对该胎儿的二维和三维扫描确定了由于早期多种事件共同作用导致的器官移位。