THE EARLY PRENATAL SONOGRAPHIC DIAGNOSIS OF RENAL AGENESIS - TECHNIQUES AND POSSIBLE PITFALLS

被引:38
作者
BRONSHTEIN, M
AMIT, A
ACHIRON, R
NOY, I
BLUMENFELD, Z
机构
[1] TECHNION ISRAEL INST TECHNOL, BRUCE RAPPAPORT FAC MED, RAMBAM MED CTR, DEPT OBSTET & GYNECOL A, IL-31096 HAIFA, ISRAEL
[2] RAMBAM MED CTR, DEPT OBSTET & GYNECOL, IL-31096 HAIFA, ISRAEL
[3] CHAIM SHEBA MED CTR, IL-52621 TEL HASHOMER, ISRAEL
[4] HILLEL YAFFE MED CTR, HADERA, ISRAEL
关键词
RENAL AGENESIS; FETAL KIDNEY MALFORMATIONS; POTTER SYNDROME; HYPOECHOGENIC KIDNEYS; FETAL SONOGRAPHY;
D O I
10.1002/pd.1970140409
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Out of 13 252 cases in which fetal bilateral echogenic kidneys were detected by transvaginal sonography between 12 and 18 weeks' gestation, there were nine fetuses where oval hypoechogenic masses were detected in the renal bed. In five fetuses where hypoechogenic masses in the renal bed were sonographically visualized, postabortal examination was compatible with renal agenesis and the hypoechogenic masses proved to be enlarged adrenals. In three additional cases, unilateral renal agenesis was accompanied by unilateral enlarged adrenals, radiologically confirmed postnatally. In one case, a false-positive sonographic diagnosis of Potter syndrome was made because of bilateral hypoechogenic masses in the renal bed. Postabortal examination detected hypoplastic kidneys, but of normal histology, in a dyskaryotic fetus with trisomy 22. In four cases of renal agenesis, the amniotic fluid was of normal volume until the 17th week. In two of the five cases of Potter syndrome, a cystic structure, compatible with the urinary bladder, was detected in the pelvis at 14 weeks. The diagnostic criteria for renal agenesis in the early fetus differ from those used in the second half of gestation.
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页码:291 / 297
页数:7
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