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MRI of Fetal Genitourinary Anomalies

Jacqueline T. Caire1, Ronald M. Ramus2, Kevin P. Magee2, Bryan K. Fullington1, David H. Ewalt3 and Diane M. Twickler1,2

1 Department of Radiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-8896.
2 Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390-8896.
3 Perinatal Associates of Texas, Ste. 205, 8315 Walnut Hill Ln., Dallas, TX 75230-5104.



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Fig. 1A. 35-gestational-week-old fetus with suspected renal agenesis, which occurs if metanephric diverticulum fails to develop or to penetrate metanephric blastema. Coronal MRI obtained through fetus shows bright fluid in stomach (white arrow) and psoas muscles (black arrows), but no kidneys are identified.

 


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Fig. 1B. 35-gestational-week-old fetus with suspected renal agenesis, which occurs if metanephric diverticulum fails to develop or to penetrate metanephric blastema. Axial MRI of fetal abdomen reveals large anterior mass thought to represent single abnormal lower extremity (large straight arrow), but no kidneys, on either side of spinal column (small straight arrow). Placenta (curved arrows) abuts fetus because of anhydramnios.

 


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Fig. 1C. 35-gestational-week-old fetus with suspected renal agenesis, which occurs if metanephric diverticulum fails to develop or to penetrate metanephric blastema. Photograph of stillborn neonate displays appearance of sirenomelia.

 


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Fig. 2. Cystic areas (arrows) are bright on coronal T2-weighted image of 31-gestational-week-old fetus with bilateral multicystic dysplastic kidneys.

 


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Fig. 3. T2-weighted image obtained with single-shot fast spin-echo sequence in 25-gestational-week-old fetus with left ureteropelvic junction obstruction and retroperitoneal urinoma. Urine and urinoma appear bright. Dilated left renal pelvis (arrows) is shown in axial plane, deviated to midline by large urinoma (u).

 


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Fig. 4A. 30-gestational-week-old female fetus with duplicated right collecting system, which is caused by second ureteral bud arising from mesonephric duct. Coronal MRI obtained through fetus reveals that upper moiety of pole is dilated on right (thin white arrows), whereas lower moiety of right kidney pole displays mild dilatation of renal pelvis (thick white arrow). Left kidney appears normal (black arrow).

 


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Fig. 4B. 30-gestational-week-old female fetus with duplicated right collecting system, which is caused by second ureteral bud arising from mesonephric duct. Sagittal MRI of perineum of fetus shows dilated ureterocele in region of vagina (arrow) with associated ureteral dilatation (arrowheads).

 


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Fig. 4C. 30-gestational-week-old female fetus with duplicated right collecting system, which is caused by second ureteral bud arising from mesonephric duct. Axial MRI obtained at level of perineum shows vaginal ectopic ureterocele (large arrow) and thighs (small arrows) anteriorly.

 


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Fig. 4D. 30-gestational-week-old female fetus with duplicated right collecting system, which is caused by second ureteral bud arising from mesonephric duct. Photograph shows neonate's external perineum with ureterocele (arrows) pulled inferiorly by surgeon as well as relationship of ureterocele to vaginal walls.

 


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Fig. 5A. MRI of megacystis-microcolon–intestinal hypoperistalsis syndrome in 30-gestational-week-old female fetus. b = bladder. Sagittal MRI obtained through fetal abdomen and pelvis reveals massively dilated bladder and renal hydronephrosis (arrow).

 


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Fig. 5B. MRI of megacystis-microcolon–intestinal hypoperistalsis syndrome in 30-gestational-week-old female fetus. b = bladder. Axial MRI obtained through mid abdomen shows large bladder and bilateral hydronephrosis (arrows).

 


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Fig. 6A. 34-gestational-week-old fetus with cloacal exstrophy. Axial MRI obtained through fetal abdomen shows anterior omphalocele (long arrows) and posterior myelocystocele (short arrow).

 


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Fig. 6B. 34-gestational-week-old fetus with cloacal exstrophy. Axial MRI of perineal region shows hemibladders (arrows) and bladder exstrophy. Anus is absent.

 


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Fig. 6C. 34-gestational-week-old fetus with cloacal exstrophy. Sagittal MRI obtained through fetus shows extensive fetal malformations including myelocystocele (black arrow), hemibladder (white open arrow), and omphalocele (white solid arrows).

 


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Fig. 6D. 34-gestational-week-old fetus with cloacal exstrophy. Coronal T2-weighted image of lumbosacral spine shows dilated distal spinal canal with bright signal, suggestive of myelocystocele.

 


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Fig. 6E. 34-gestational-week-old fetus with cloacal exstrophy. Photograph of lower abdomen of neonate reveals anterior open defect (straight arrows) and hemibladder (curved arrows).

 

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