Fetal Pancake Kidney Prenatal Diagnosis and Postnatal Follow-up

被引：4

作者：

Perlman, Sharon ^{[1
,2
]}

Borovitz, Yael ^{[2
,3
]}

Bar-Adon, Sonya ^{[2
,4
]}

Dekel, Benjamin ^{[2
,5
,6
]}

Achiron, Reuven ^{[2
,4
]}

Gilboa, Yinon ^{[1
,2
]}

机构：

[1] Rabin Med Ctr, Helen Schneider Womens Hosp, Ultrasound Unit, 39 Jabotinski St, IL-49100 Petah Tiqwa, Israel

[2] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel

[3] Schneider Childrens Med Ctr, Nephrol Inst, Petah Tiqwa, Israel

[4] Chaim Sheba Med Ctr, Prenatal Diagnost Unit, Dept Obstet & Gynecol, Tel Hashomer, Israel

[5] Chaim Sheba Med Ctr, Edmond & Lily Childrens Hosp, Div Pediat Nephrol, Tel Hashomer, Israel

[6] Chaim Sheba Med Ctr, Edmond & Lily Childrens Hosp, Pediat Stem Cell Res Inst, Tel Hashomer, Israel

来源：

JOURNAL OF ULTRASOUND IN MEDICINE | 2020年 / 39卷 / 08期

关键词：

congenital anomalies of the kidney and urinary tract; Mayer-Rokitansky-Kuster-Hauser syndrome; pancake kidney; prenatal diagnosis; prenatal ultrasound; SINGLE URETER; CHILDREN;

D O I：

10.1002/jum.15251

中图分类号：

O42 [声学];

学科分类号：

070206 ; 082403 ;

摘要：

Bilateral failure of the kidneys to ascend during embryonic life may lead to fusion of the two renal masses, resulting in a round mass known as pancake kidney. Reviewing the literature, we did not encounter any reports of prenatal diagnosis of pancake kidneys. We present 6 cases of a pancake kidney diagnosed prenatally. Extrarenal associated anomalies included an aberrant right subclavian artery, nonvisualization of the uterus, consistent with Mayer-Rokitansky-Kuster-Hauser syndrome, and a sequence of early-onset growth restriction, hypospadias, and syndactyly, suspected as Smith-Lemli-Opitz syndrome. On postnatal follow-up, all infants had a normal renal outcome.

引用

页码：1665 / 1668

页数：4

共 29 条

[1] Is a complete urological evaluation necessary in all newborns with asymptomatic renal ectopia? [J].