Diagnostic value of fetal MRI in evaluating fetal urinary anomalies

Diagnostic value of fetal MRI in evaluating fetal urinary anomalies
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DOI:
10.1016/j.ejrnm.2014.11.015
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发表时间:
2015-06-01
影响因子:
1
通讯作者:
Ali, Mohamed Abd El Kader
Ali, Mohamed Abd El Kader
中科院分区:
其他
文献类型:
--
作者:
Behairy, Noha Hosam El Din;El Din, Lamiaa Adel Salah;Ali, Mohamed Abd El Kader

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目的:通过对30例超声诊断为先天性尿路畸形的胎儿进行二维/三维超声及MRI检查,探讨胎儿MRI诊断尿路异常的准确性。胎龄18~36周。43%的妇女处于中期妊娠。结果:双侧常染色体隐性遗传性多囊肾病8例,单侧常染色体隐性遗传性多囊肾病1例,肾集合系统扩张8例,肾发育不全3例,双侧多囊肾增大5例,单侧增大多囊发育不良肾4例,肾发育不良1例。MRI改变超声诊断6例,增加信息4例。3例MRI改变了患者的治疗方法。核磁共振检查证实了20例胎儿的超声诊断。1例肾功能衰竭患者超声检查优于MRI检查。伴发肾外异常9例(30%)。MRI诊断准确率为96%。死亡率达56%。结论:胎儿MRI可作为超声诊断不明或可疑胎儿尿路异常的补充手段。(C)2014年埃及放射和核医学学会。
Purpose: To detect the accuracy of fetal MRI in diagnosing urinary tract anomalies in comparison with ultrasonographic findings and fetal outcome.Methods: We examined 30 fetuses with sonographically suspected congenital urinary tract anomalies by 2D/3D ultrasound and MRI. The gestational age range was 18-36 weeks. 43% of the women were in the second trimester. The diagnosis was confirmed by postnatal ultrasound, cystogram and biopsy in born babies and autopsy in still born or abortus fetuses.Results: We found different urinary tract anomalies including: bilateral autosomal recessive polycystic kidney disease (n = 8), unilateral autosomal recessive polycystic kidney disease (n = 1), dilated collecting system (n = 8), renal agenesis (n = 3), bilateral enlarged multicystic dysplastic kidneys (n = 5), unilateral enlarged multicystic dysplastic kidney (n = 4) and renal dysplasia (n = 1). MRI changed the US diagnosis in 6 cases and added information in 4 cases. MRI changed the patient's management in 3 cases. MRI confirmed US diagnosis in 20 fetuses. Ultrasound was superior to MRI in one case of renal failure. Associated extrarenal anomalies were detected in 9 cases (30%). MRI showed 96% accuracy in diagnosis. Mortality rate reached 56%.Conclusion: Fetal MR imaging may be used as a complementary modality to US in diagnosing inconclusive or equivocal fetal urinary abnormality. (C) 2014 The Egyptian Society of Radiology and Nuclear Medicine.