Department of Obstetrics and Gynecology, Shaare Zedek Medical Center, Jerusalem, Israel.
Ultrasound Obstet Gynecol. 2011 Jun;37(6):673-7. doi: 10.1002/uog.8861. Epub 2011 May 9.
Fetal gallbladder non-visualization on prenatal ultrasound in the second trimester is uncommon and in most cases the gallbladder is detected eventually. Associations of gallbladder non-visualization with cystic fibrosis, aneuploidy, agenesis of the gallbladder and biliary atresia have been reported. We present our experience and review the literature.
During the study period from January 2004 to June 2009 we collected prospectively cases of non-visualization of the fetal gallbladder in the second trimester. In each case the fetus was evaluated by two examiners on at least two occasions, at least a week apart. Cases with no additional sonographic malformations were designated as isolated. Further evaluation included follow-up scans and a meticulous search for fetal anomalies. All patients were offered genetic consultation. Cystic fibrosis testing, amniocentesis for karyotyping and analysis of fetal digestive enzymes in the amniotic fluid were offered.
We collected 21 cases of non-visualization of the fetal gallbladder, 16 of which were isolated and five of which had additional malformations. In four of these five, the associated anomalies were severe and the pregnancies were terminated for aneuploidy (two cases of trisomy 18 and one triploidy) or for the severity of the associated anomalies. Associated anomalies included left isomerism with complex cardiac anomaly and intrauterine growth restriction with multisystem anomalies. The fifth fetus had interrupted inferior vena cava with azygos continuation without other anomalies and the child was alive and well at the age of 4 years. In 15 of the 16 isolated cases, antenatal and postnatal development were normal at the last follow-up, ranging from 4 months to 2.5 years. One case of cystic fibrosis was diagnosed prenatally and this pregnancy was terminated. There were no diagnoses of abnormal karyotype or biliary atresia among cases of isolated non-visualization of the gallbladder.
When prenatal non-visualization of the fetal gallbladder is associated with other severe malformation, aneuploidy should be suspected. When it is isolated, if cystic fibrosis is ruled out, the outcome is good.
胎儿在妊娠中期的产前超声胆囊未显示并不常见,且多数情况下最终会检测到胆囊。已有报道称,胆囊未显示与囊性纤维化、非整倍体、胆囊发育不全和胆道闭锁相关。我们在此呈现我们的经验并回顾文献。
在 2004 年 1 月至 2009 年 6 月的研究期间,我们前瞻性地收集了妊娠中期胎儿胆囊未显示的病例。在每例病例中,由至少两名检查者在至少两次、间隔至少一周的检查中对胎儿进行评估。如果没有其他超声畸形,则将病例指定为孤立性。进一步评估包括随访扫描和对胎儿畸形的细致检查。所有患者均提供遗传咨询。囊性纤维化检测、羊水核型分析和胎儿消化酶分析可用于评估。
我们共收集了 21 例胎儿胆囊未显示的病例,其中 16 例为孤立性,5 例存在其他畸形。在这 5 例中,有 4 例存在严重的相关畸形,由于非整倍体(2 例 18 三体和 1 例三倍体)或相关畸形的严重程度而终止妊娠。相关畸形包括左异构伴复杂心脏异常和宫内生长受限伴多系统异常。第 5 例胎儿存在下腔静脉中断伴奇静脉延续,无其他异常,目前 4 岁,情况良好。在 16 例孤立性病例中,有 15 例在最后一次随访时产前和产后发育正常,随访时间从 4 个月到 2.5 岁不等。1 例产前诊断为囊性纤维化,该妊娠被终止。孤立性胆囊未显示病例中未发现异常核型或胆道闭锁的诊断。
当产前胎儿胆囊未显示与其他严重畸形相关时,应怀疑存在非整倍体。当胆囊未显示为孤立性时,如果排除囊性纤维化,结局通常较好。