Kitagawa H, Pringle K C, Stone P, Flower J, Murakami N, Robinson R
Department of Surgery, Wellington School of Medicine, New Zealand.
Fetal Diagn Ther. 1998 Jan-Feb;13(1):19-25. doi: 10.1159/000020795.
Babies with hydronephrosis detected antenatally who were born at or referred to our hospital from 1990 to 1995 were followed up with ultrasound (U/S), micturating cystourethrogram (MCU) or nuclear medicine studies after birth. One hundred and three patients were diagnosed antenatally at 17-42 weeks gestation. Twelve cases were excluded from the analysis of the results because of incomplete data. Fifty-one (56%) patients had hydronephrosis without organic obstruction, and 80% of these became normal in 3 years. Fifteen patients (17%) had a normal scan 4 days after birth. This suggests the possibility of antenatal spontaneous regression. Seven (8%) had a ureterocele and 4 (5%) had pelviureteric junction (PUJ) obstruction. Four (5%) had vesicoureteric reflux, and 4 (5%) had primary megaureter. Two (2%) had posterior urethral valves (PUV), 3 (3%) had refluxing primary megaureter, and 1 (1%) had urethral atresia. Fifteen patients (17%) underwent surgical intervention. Six had a nephrectomy, 1 a vesicostomy, 3 an Anderson-Hynes pyeloplasty, 3 had the ureterocele unroofed, 1 had a ureteric reimplant, and 1 ablation of valves. In 42 infants with 60 abnormal kidneys, the renal anteroposterior diameter of the pelvis was measured. Retrospectively, 48 kidneys diagnosed as having hydronephrosis, antenatally had a renal pelvis diameter > or = 4 mm before 33 weeks gestation or > or = 7 mm after 33 weeks gestation. One patient with PUJ obstruction lost kidney function, but there is no good marker to detect these patients. Early unroofing of ureteroceles may rescue kidney function. Our follow-up protocol for antenatal hydronephrosis is U/S at 4 days, 1 month and 1 year of age. An MCU is not required unless the ureter is seen on antenatal U/S. If dilatation persists past 1 month, a radionucleotide (MAG3) scan and repeat U/S are performed at 3 months. The methods for assessing obstruction and the indications for surgical intervention in these patients require reexamination.
1990年至1995年期间在我院出生或转诊至我院的产前诊断为肾积水的婴儿,出生后接受了超声(U/S)、排尿性膀胱尿道造影(MCU)或核医学检查随访。103例患者在妊娠17 - 42周时被产前诊断。12例因数据不完整被排除在结果分析之外。51例(56%)患者有肾积水但无器质性梗阻,其中80%在3年内恢复正常。15例患者(17%)出生后4天扫描结果正常。这提示产前自发消退的可能性。7例(8%)有输尿管囊肿,4例(5%)有肾盂输尿管连接处(PUJ)梗阻。4例(5%)有膀胱输尿管反流,4例(5%)有原发性巨输尿管。2例(2%)有后尿道瓣膜(PUV),3例(3%)有反流性原发性巨输尿管,1例(1%)有尿道闭锁。15例患者(17%)接受了手术干预。6例行肾切除术,1例行膀胱造瘘术,3例行安德森 - 海恩斯肾盂成形术,3例进行输尿管囊肿开窗术,1例行输尿管再植术,1例进行瓣膜切除术。对42例有60个异常肾脏的婴儿测量了肾盂前后径。回顾性分析,产前诊断为肾积水的48个肾脏,在妊娠33周前肾盂直径≥4 mm或妊娠33周后≥7 mm。1例PUJ梗阻患者肾功能丧失,但尚无检测这些患者的良好指标。早期输尿管囊肿开窗术可能挽救肾功能。我们对产前肾积水的随访方案是在出生后4天、1个月和1岁时进行超声检查。除非产前超声检查发现输尿管,否则不需要进行排尿性膀胱尿道造影。如果扩张持续超过1个月,在3个月时进行放射性核素(MAG3)扫描并重复超声检查。评估这些患者梗阻的方法和手术干预的指征需要重新审视。