Bronshtein M, Weiner Z, Abramovici H, Filmar S, Erlik Y, Blumenfeld Z
Al-Kol Institute of Sonography, Haifa, Israel.
Prenat Diagn. 1993 Sep;13(9):851-61. doi: 10.1002/pd.1970130909.
We describe here 17 cases of fetal gall bladder anomalies, detected as early as the 14th week of gestation, out of 10,016 fetal systemic examinations performed by us in the last 6 years (0.15 per cent). In seven cases, agenesis of the fetal gall bladder was detected. The diagnosis was confirmed by post-abortal examination in five cases and in two post-partum. In six other cases, a left-sided gall bladder and in one case, a 'floating' gall bladder were detected at 15 weeks' gestation. In two cases, a septated or bilobed gall bladder was visualized. None of these 15 cases was dyskaryotic, but in five cases, two with agenesis and three left-sided gall bladders were associated with other fetal malformations. In two other cases, the gall bladder appeared dysmorphic on sonographic examination and in both of them intrauterine growth retardation and other anomalies were detected. Trisomy 18 was diagnosed by amniocentesis in one of them. According to our experience, failure to visualize the fetal gall bladder by the 15th gestational week is diagnostic of its absence and should raise the differential diagnosis between gall bladder atresia, which has a good prognosis, and external biliary atresia, which has a poor prognosis. Further experience is needed to characterize the various gall bladder malformations and their prognosis.
我们在此描述了17例胎儿胆囊异常病例,这些病例早在妊娠第14周时就被检测到,是我们在过去6年对10016例胎儿进行全身检查时发现的(占0.15%)。其中7例检测到胎儿胆囊缺如。5例经流产后检查、2例经产后检查确诊。另外6例在妊娠15周时检测到左侧胆囊,1例检测到“漂浮”胆囊。2例可见分隔或双叶胆囊。这15例中均未发现核异常,但5例,其中2例胆囊缺如、3例左侧胆囊伴有其他胎儿畸形。另外2例超声检查显示胆囊形态异常,均检测到宫内生长受限及其他异常。其中1例经羊水穿刺诊断为18三体综合征。根据我们的经验,在妊娠第15周仍未观察到胎儿胆囊可诊断为胆囊缺如,应进一步鉴别预后良好的胆囊闭锁和预后不良的肝外胆管闭锁。还需要更多经验来明确各种胆囊畸形及其预后情况。