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1. 12/14/2011 L.Zanin - MS213 - GU 1 Fetal Genitourinary System
2. 12/14/2011 L.Zanin - MS213 - GU 2
3. 12/14/2011 L.Zanin - MS213 - GU 3 Genitourinary System Rule of thumb - during the second and third trimesters the kidneys increase in length at approximately 1 mm per week and increase in AP diameter .5 mm per week
The normal ureter is not seen sonographically
The normal adrenal gland can be visualized at the superior border of the kidney
4. 12/14/2011 L.Zanin - MS213 - GU 4 Genitourinary System Although the fetal kidneys are functionally immature throughout fetal life, urine production in the fetus begins by 10 weeks gestation
However fetal urine does not become the primary source of amniotic fluid volume until 16-18 weeks gestation
5. 12/14/2011 L.Zanin - MS213 - GU 5 Fetal Kidneys in Transverse Spine up position
Notice the renal pelvis's which are filled with urine
The stomach is found anterior to the left kidney
Notice the spine shadow
6. 12/14/2011 L.Zanin - MS213 - GU 6 Renals in Sagittal Prominent renal pyramids are normal in the fetus and newborn.
This is where you would measure the renal size.
7. 12/14/2011 L.Zanin - MS213 - GU 7 Fetal kidney
8. 12/14/2011 L.Zanin - MS213 - GU 8 Normal Kidney
9. 12/14/2011 L.Zanin - MS213 - GU 9 Adrenal Gland It is observed in a sagittal view and is located above the kidney
The adrenal gland is often mistaken for the kidney with renal agenesis
Notice the dense central interface
10. 12/14/2011 L.Zanin - MS213 - GU 10 Normal Kidney - Adrenal
11. 12/14/2011 L.Zanin - MS213 - GU 11 Renal Anomalies At approximately six menstrual weeks the ureteral bud develops from the urogenital sinus
It then develops into the ureter, renal pelvis, calyces and collecting tubules
The ureteral bud also contributes to the development of the nephron
If there is no ureteral bud, no kidney will develop
12. 12/14/2011 L.Zanin - MS213 - GU 12 Sagittal Kidney
13. 12/14/2011 L.Zanin - MS213 - GU 13 Transverse Kidneys
14. 12/14/2011 L.Zanin - MS213 - GU 14 Sagittal Kidneys
15. 12/14/2011 L.Zanin - MS213 - GU 15 Potters Syndrome Is the result of severe oligohydramnios
The anomalies associated with potters syndrome are due to the long-standing severe oligohydramnios
The term Potters Syndrome is now referred to as Potters Sequence or Oligohydramnios Sequence
Lungs become hypoplastic which may lead to death from pulmonary insufficiency at birth
16. 12/14/2011 L.Zanin - MS213 - GU 16 Potters Syndrome Facial abnormalities include
Fold of skin above each eye that extends over the inner cheek, low set ears and a turned down nose
Limb abnormalities include
Abnormal positioning of hands and feet, hyperextension or bowing of legs, clubbed or fused feet, & hip dislocation
17. 12/14/2011 L.Zanin - MS213 - GU 17 Potters Syndrome
18. 12/14/2011 L.Zanin - MS213 - GU 18 Renal Agenesis One subclassification of Potter’s Syndrome it consists of:
Bilateral renal agenesis
Pulmonary hypoplasia
Facial anomalies
Absence of the ureteral bud to form this causes bilateral renal agenesis and death from pulmonary hypoplasia
Sonographicly - severe oligohydramnios will be seen with associated anomalies
Non-visualization of the bladder is more important then suspected absence of the kidneys because the adrenal may be mistaken for kidneys
19. 12/14/2011 L.Zanin - MS213 - GU 19 Renal Agenesis Fatal prognosis with an occurrence of 1 in 3,000 births
Male predominance of 2.5 to 1
Absence of the fetal urine production initiates the Potter sequence
Absence of the urinary bladder
Unilateral renal agenesis is 3-4 times more frequent than bilateral, and it is compatible with life
20. 12/14/2011 L.Zanin - MS213 - GU 20 No Renal Arteries
21. 12/14/2011 L.Zanin - MS213 - GU 21 Ultrasound Findings No kidneys or bladder seen with bilateral renal agenesis (must see kidneys by 17-22 weeks and bladder must be seen by 12 wk.
Severe oligohydramnios
Fetal thorax is abnormally small
Unilateral agenesis is rarely associated with oligohydramnios or nonvisualization of the fetal bladder
22. 12/14/2011 L.Zanin - MS213 - GU 22 Renal Agenesis
23. 12/14/2011 L.Zanin - MS213 - GU 23 Unilateral Renal Agenesis Occurs more often than bilateral
Incidence is 1 in 500
It occurs more commonly on the left than the right side
Male predominance of 1.8 to 1
Diagnosed by seeing one kidney, but one has to be careful to evaluate for an ectopic kidney
24. 12/14/2011 L.Zanin - MS213 - GU 24 Unilateral Renal Agenesis Fluid will be seen in the bladder and normal amniotic fluid volumes should be seen
Associated anomalies involving the genital tract are common
25. 12/14/2011 L.Zanin - MS213 - GU 25 Unilateral Renal Agenesis Transverse view of a 37 week fetus demonstrating a normal left kidney and no right kidney
26. 12/14/2011 L.Zanin - MS213 - GU 26 Unilateral Renal Artery
27. 12/14/2011 L.Zanin - MS213 - GU 27 Hypoplastic Kidney Failure of a kidney to develop to their normal size
More commonly unilateral
Ultrasound appearance - small echogenic kidney
28. 12/14/2011 L.Zanin - MS213 - GU 28 Ectopic Kidney Can be found in the pelvis, iliac, abdomen, thorax and contralateral side
Incidence is 1 in 500 births with no predominance in either sex
It is slightly more common on the left side
Ectopic kidneys are associated with an increased incidence of contralateral agenesis and with genitalia anomalies
29. 12/14/2011 L.Zanin - MS213 - GU 29 Ectopic Kidney Sagittal view through the pelvis demonstrating a pelvic right kidney
30. 12/14/2011 L.Zanin - MS213 - GU 30 Ectopic kidney
31. 12/14/2011 L.Zanin - MS213 - GU 31 Ectopic kidney
32. 12/14/2011 L.Zanin - MS213 - GU 32 Multicystic Dysplastic Kidney(MDK) Most common cause of an abdominal mass in the neonate
Usually unilateral, sometimes bilateral
Development of enlarged kidneys containing encapsulated cysts of varying sizes
Cysts distort the renal parenchyma & there is NO communication between the cysts
Found in 1 out of 3000 births
33. 12/14/2011 L.Zanin - MS213 - GU 33 Multicystic Dysplastic Kidney In MDK the normal renal parenchyma is totally replaced by cysts of different sizes
This anomaly most likely occurs during embryogenesis, resulting from atresia of the ureteral bud system
Causes severe oligohydramnios when seen bilaterally
When unilateral - monitored closely
When bilateral - neonatal demise will follow
34. 12/14/2011 L.Zanin - MS213 - GU 34 Multicystic Dysplastic Kidney(MDK) C-section is usually done
The involved renal tissue has little or no function
When unilateral contralateral renal anomalies are present in 40%
Prognosis - good if unilateral, if bilateral it is fatal
35. 12/14/2011 L.Zanin - MS213 - GU 35 MDK Ultrasound Findings Potter’s type II classifications:
A – normal or enlarged kidney
B- small aplastic kidney
Enlarged kidney(s) with multiple cysts
The abdominal circumference is enlarged
Renal contour is generally distorted
Unilateral
Amniotic fluid is normal, multiple cysts in one kidney, bladder is seen
Bilateral
Fetal bladder is not visualized, severe oligohydramnios, Multiple cysts in both kidneys
36. 12/14/2011 L.Zanin - MS213 - GU 36 Unilateral MDK Right fetal kidney demonstrates multiple cysts of varying sizes that do not communicate with the renal pelvis
37. 12/14/2011 L.Zanin - MS213 - GU 37 MDK
38. 12/14/2011 L.Zanin - MS213 - GU 38 MDK
39. 12/14/2011 L.Zanin - MS213 - GU 39 Multicystic Dysplastic Kidney
40. 12/14/2011 L.Zanin - MS213 - GU 40 MDK
41. 12/14/2011 L.Zanin - MS213 - GU 41 MDK
42. 12/14/2011 L.Zanin - MS213 - GU 42 MDK
43. 12/14/2011 L.Zanin - MS213 - GU 43 Multicystic Dysplastic Kidney
44. 12/14/2011 L.Zanin - MS213 - GU 44 Multicystic Dysplastic Kidney
45. 12/14/2011 L.Zanin - MS213 - GU 45 Multicystic Dysplastic Kidney
46. 12/14/2011 L.Zanin - MS213 - GU 46 Polycystic Kidney Disease Autosomal Recessive PKD - Formally known as Infantile (IPKD) (differentiate from Autosomal Dominant APKD)
Bilateral dilation of the collecting tubules in the kidneys due to an chromosomal recessive gene
Associated with liver fibrosis, microcephaly, & ambiguous genitalia
Incidence is 1 in 16,000 births
47. 12/14/2011 L.Zanin - MS213 - GU 47 IPKD Oligohydramnios is present due to the diminished urine production this initiates the Potter sequence and death may occur shortly after birth from pulmonary hypoplasia
It can be present after birth, however, the later the presentation the less severe the renal involvement & the more severe the hepatic involvement
48. 12/14/2011 L.Zanin - MS213 - GU 48 Ultrasound Findings Can be detected as early as 17 weeks
Echogenic multiple tiny cysts
2 echogenic enlarged kidneys
Oligohydramnios
Renal contour is generally maintained
Bladder is frequently not visualized
This anomaly is a major feature of the Meckel syndrome hence there would be other associated anomalies
49. 12/14/2011 L.Zanin - MS213 - GU 49 Infantile Polycystic Kidney 21 week fetal abdomen demonstrates enlarged echogenic kidneys that maintain a renal shape
50. 12/14/2011 L.Zanin - MS213 - GU 50 Polycystic Kidneys
51. 12/14/2011 L.Zanin - MS213 - GU 51 Bilateral Polycystic Kidney
52. 12/14/2011 L.Zanin - MS213 - GU 52 IPKD
53. 12/14/2011 L.Zanin - MS213 - GU 53 Meckel-Gruber Syndrome A group of anomalies associated with bilateral markedly enlarged echogenic kidneys with small cysts (Not Typically Seen) associated with IPKD
Other anomalies associated with this syndrome include
Encephalocele
Polydactyly
Ambiguous external genitalia in males
54. 12/14/2011 L.Zanin - MS213 - GU 54 Meckel-Gruber Syndrome
55. 12/14/2011 L.Zanin - MS213 - GU 55 Meckel-Gruber Syndrome
56. 12/14/2011 L.Zanin - MS213 - GU 56 Meckel-Gruber Syndrome
57. 12/14/2011 L.Zanin - MS213 - GU 57 Beckwith-Wiedeman Syndrome The syndrome results in the combination of the following conditions together
Macrosomia
Protruding tongue
Enlarged kidneys
Omphalocele
58. 12/14/2011 L.Zanin - MS213 - GU 58 Beckwith-Wiedeman Syndrome Protruding Tongue
59. 12/14/2011 L.Zanin - MS213 - GU 59 Beckwith-Wiedeman Syndrome Protruding Tongue
60. 12/14/2011 L.Zanin - MS213 - GU 60 Beckwith-Wiedeman Syndrome
61. 12/14/2011 L.Zanin - MS213 - GU 61 Renal Vein Thrombosis Results in varying degrees of renal failure
Often caused by maternal diabetes
Kidneys appear enlarged
62. 12/14/2011 L.Zanin - MS213 - GU 62 Renal Vein Thrombosis This diabetic mother has a 3rd trimester fetus with echogenic kidneys and calficications due to bilateral renal vein thrombosis.
63. 12/14/2011 L.Zanin - MS213 - GU 63 Hydronephrosis Hydronephrosis - an obstructed kidney with a dilated collecting system
Occurs during early fetal development
Caused by a partial ureteral obstruction with a distention of the renal pelvis and calyces
Sonographicly - excess collection of fluid within the renal pelvis, diminished urinary output in the fetus & oligohydramnios
64. 12/14/2011 L.Zanin - MS213 - GU 64 Hydronephrosis Most common fetal renal abnormality
Usually an incidental finding
May be caused by obstruction or reflux which causes dilation of the ureters and renal pelvis
Oligohydramnios will be seen depending on the severity of the obstruction
The sites of obstruction include ureteropelvic junction, ureter, ureterovesicle junction, and urethra
65. 12/14/2011 L.Zanin - MS213 - GU 65 Hydronephrosis If the AP diameter of the renal pelvis is greater than 50% of the the AP diameter of the kidney this indicates hydronephrosis
The renal pelvis is considered normal if they measure up to 4 mm prior to 33 weeks and up to 7 mm after 33 weeks
66. 12/14/2011 L.Zanin - MS213 - GU 66 Hydronephrosis
67. 12/14/2011 L.Zanin - MS213 - GU 67 Hydronephrosis
68. 12/14/2011 L.Zanin - MS213 - GU 68 Hydronephrosis
69. 12/14/2011 L.Zanin - MS213 - GU 69 Hydronephrosis Mild pelviectasis and calyceal dilatation
70. 12/14/2011 L.Zanin - MS213 - GU 70 Pyelectasis In a transverse plane, measure the AP diameter
If the dilation is less than 1 cm and a ratio of pelvic to kidney diameter is less than 50% than the fluid within the pelvis is considered within normal limits
Rule of thumb - AP diameter of the reanl pelvis should be no greater than 4-5 mm prior to 33 weeks and no greater than 7mm-1 cm after 33 weeks
71. 12/14/2011 L.Zanin - MS213 - GU 71 Pyelectasis
72. 12/14/2011 L.Zanin - MS213 - GU 72 Pyelectasis
73. 12/14/2011 L.Zanin - MS213 - GU 73 Ureteropelvic Junction (UPJ) UPJ - ureteropelvis junction obstruction (ureter is not dilated)
1/3 of the cases are bilateral
Most common congenital cause of obstructive uropathy, representing 2/3 of fetal hydronephrosis
UPJ obstructions are more often unilateral
Causes include:
Fibrous adhesions
Kinks
Ureteral valves
74. 12/14/2011 L.Zanin - MS213 - GU 74 Ureteropelvic Junction (UPJ) More common in males with a 2:1 ratio
UPJ obstruction can result in rupture of the collecting system and the development of a urinoma
If the UPJ is unilateral the bladder and amniotic fluid will be normal
75. 12/14/2011 L.Zanin - MS213 - GU 75 UPJ Bilateral severe UPJ obstruction-dilated renal pelvis
76. 12/14/2011 L.Zanin - MS213 - GU 76 UPJ
77. 12/14/2011 L.Zanin - MS213 - GU 77 Ultrasound Findings Dilatation of the renal pelvis with varying degrees of caliectasis
Normal ureter and bladder
Renal cortex may be normal or thin
The amount of amniotic fluid is usually normal if unilateral however it may be decreased if the obstruction is severe or bilateral
78. 12/14/2011 L.Zanin - MS213 - GU 78 Uretero Vesicle Junction Obstruction (UVJ) UVJ - uretero vesicle junction obstruction, there is an obstruction where the ureter enters the bladder
Rare & typically due to a renal duplication anomaly
Unilateral hydronephrosis & hydroureter
79. 12/14/2011 L.Zanin - MS213 - GU 79 Uretero Vesicle Junction Obstruction (UVJ) The bladder is usually normal
Amniotic fluid volume is generally normal
More commonly found on the left side & more common in males
Depending on severity, it can result in dilation of the ureter with or without hydro
80. 12/14/2011 L.Zanin - MS213 - GU 80 UVJ Differential diagnosis:
Bowel obstruction
Dilated ureter secondary to bladder dysfunction
A dilated tortuous tubular structure that showed no peristalsis that can be traced back to the renal pelvis = UVJ
81. 12/14/2011 L.Zanin - MS213 - GU 81 UVJ
82. 12/14/2011 L.Zanin - MS213 - GU 82 UVJ
83. 12/14/2011 L.Zanin - MS213 - GU 83 UVJ
84. 12/14/2011 L.Zanin - MS213 - GU 84 Posterior Urethral Valves (PUV) An urethral obstruction seen in males
Most common cause of urinary obstruction in male infants
Retrograde filling of the bladder, dilation of bladder, ureters & renal pelvis
Can cause severe damage to kidneys, ureters and bladder
Prognosis is poor when associated with oligo
The ureter is dilated (hydroureter) above the obstruction and is not visualized below it
85. 12/14/2011 L.Zanin - MS213 - GU 85 Posterior Urethral Valves (PUV) Peristalsis may be noted in the upper ureter
The valves are redundant folds of urethral mucosa that cause varying degrees of obstruction
Bladder wall thickening is seen
Marked hydronephrosis and dilated ureter, dilated posterior urethra and bladder
86. 12/14/2011 L.Zanin - MS213 - GU 86 PUV Hydronephrosis due to a urethral valve
The upper third of the ureter is dilated
87. 12/14/2011 L.Zanin - MS213 - GU 87 PUV
88. 12/14/2011 L.Zanin - MS213 - GU 88 PUV
89. 12/14/2011 L.Zanin - MS213 - GU 89 Ureterocele Ureterocele - dilated ureter that has prolapsed into the bladder
It may be simple or ectopic
Simple - the the ureteral orifice is in its normal position and the distal end of the ureter protrudes into the bladder
Ectopic - the distal ureter does not insert into the fetal bladder but inserts ectopically
90. 12/14/2011 L.Zanin - MS213 - GU 90 Ureterocele More common in females and is generally more common on the left side
A duplicated renal collecting system is a commonly associated anomaly
The kidney on the side of the ureterocele tends to be significantly affected
91. 12/14/2011 L.Zanin - MS213 - GU 91 Ureterocele
92. 12/14/2011 L.Zanin - MS213 - GU 92 Ureterocele Ureterocele is seen protruding into a partially distended urinary bladder
93. 12/14/2011 L.Zanin - MS213 - GU 93 Ureterocele
94. 12/14/2011 L.Zanin - MS213 - GU 94 URETEROCELE
95. 12/14/2011 L.Zanin - MS213 - GU 95 URETEROCELE
96. 12/14/2011 L.Zanin - MS213 - GU 96 Bladder Outlet Obstruction Associated with severe obstructive uropathy & is most commonly caused by PUV
Bilateral hydronephrosis and hydroureters is seen
Unlike UVJ obstruction, bladder outlet obstruction is generally associated with dilatation of the proximal urethra and bladder
97. 12/14/2011 L.Zanin - MS213 - GU 97 Bladder Outlet Obstruction
98. 12/14/2011 L.Zanin - MS213 - GU 98 Bladder Outlet Obstruction
99. 12/14/2011 L.Zanin - MS213 - GU 99 Testicular Hydrocele Accumulation of fluid in the tunica vaginalis
May be due to failure of the tunica to separate fromother testicular membranes
May be associated with other GU anomalies
Frequently benign
Sonographic appearance:
Fluid surrounds the entire testicle
A small amount of fluid in the fetal scrotum is a normal finding
100. 12/14/2011 L.Zanin - MS213 - GU 100 Hydrocele Collection of fluid within the tunica vaginalis
Isolated hydrocele is not significance
101. 12/14/2011 L.Zanin - MS213 - GU 101 3 D Hydrocele
102. 12/14/2011 L.Zanin - MS213 - GU 102 Cryptorchidism Undescended Testes Can be detected by the failure to visualize the testes within the scrotum
Associated with prune belly syndrome & trisomies 13, 18, 21
If not corrected it can become cancerous
103. 12/14/2011 L.Zanin - MS213 - GU 103 Descended Testicles The scrotum outlining the descended testicles and penis are seen
104. 12/14/2011 L.Zanin - MS213 - GU 104 Descended Testicles
105. 12/14/2011 L.Zanin - MS213 - GU 105 Female Fetus The labia majora
Oreo sign
106. 12/14/2011 L.Zanin - MS213 - GU 106 Fetal Ovarian Cyst