CONGENITAL RENAL ANOMALIES: Radiological evaluation ABSTRACT NO: 143.
Fetal Renal Anomalies - North Carolina Ultrasound · PDF fileFetal Renal Anomalies-Linda...
Transcript of Fetal Renal Anomalies - North Carolina Ultrasound · PDF fileFetal Renal Anomalies-Linda...
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Linda Street MD
Maternal Fetal Medicine Fellow
Wake Forest Baptist Health
FETAL RENAL
ANOMALIES
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Fetal Renal Anomalies-Linda Street MD
I have no financial relationships to
disclose
I will not discuss off label use and/or
investigational use in my presentation
DISCLOSURES
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Discuss the components of the
Genitourinary(GU) system
Discuss basic fetal GU physiology and anatomy
Discuss normal sonographic appearances of GU
organs
Discuss GU system abnormalities
Appearance on ultrasound
Causes
Management
OBJECTIVES
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Kidneys
Ureters
Bladder
Urethra
Adrenal Glands
Internal and External genitalia
GENITOURINARY SYSTEM(GU)
COMPONENTS
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Fetal skin allows
transudation of plasma
into amniotic sac
Urine produced as early
as 9 weeks
Kidneys do not
significantly contribute to
amniotic fluid volume
prior to 16 weeks
GU SYSTEM PHYSIOLOGY
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Normal kidneys are identifiable trans-abdominally in most fetuses by 20 weeks gestation (as early as 10-12 weeks)
Normal kidneys generally span 4-5 vertebral bodies
The length of normal kidney in mm is similar to gestational age in weeks
GU SYSTEM ANATOMY
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KIDNEY ANATOMY
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LONGITUDINAL VIEW
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LONGITUDINAL VIEW
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TRANSVERSE VIEW
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TRANSVERSE VIEW
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ECTOPIC KIDNEY LOCATIONS
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PELVIC KIDNEY
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PELVIC KIDNEY1
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Abnormal Kidneys
Urinary tract dilation
Cystic kidneys
Echogenic KidneysAbsent Kidneys
Duplicated collecting
system
RENAL ANOMALIES
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AP measurement of the renal pelvis
Normal varies by gestational age
<4mm second trimester
<7mm third trimester
Present in 3% fetuses (Very common,
usually resolves)
Recently re-categorized to attempt to
standardize terminology2
URINARY TRACT DILATION(PREVIOUSLY PYELECTASIS/HYDRONEPHROSIS)
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URINARY TRACT DILATION2WHAT TO EVALUATE
US parametersMeasurement
/findingsNote
Anterior-Posterior
Renal Pelvic
Diameter
(APRPD)
(mm)
Measured on transverse
image at the maximal
diameter of intrarenal
pelvis
Calyceal dilation
Central (major
calyces)Yes/No
Peripheral
(minor calyces)Yes/No
Parenchymal
thicknessNormal/Abnormal Subjective assessment
Parenchymal
appearanceNormal/Abnormal
Evaluate echogenicity,
corticomedullary
differentiation, and for
cortical cysts
Ureter Normal/AbnormalDilation of ureter is
considered abnormal
Bladder Normal/Abnormal
Evaluate wall thickness,
for the presence of
ureterocele, and for a
dilated posterior urethra
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URINARY TRACT DILATION2
TERMINOLOGY
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URINARY TRACT DILATION2
UTD A1 (LOW RISK)
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URINARY TRACT DILATION2
UTD A2-3 (HIGH RISK)
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Etiology Incidence (%)
Transient/physiologic 50–70
Ureteropelvic junction obstruction 10–30
Vesicoureteral reflux 10–40
Ureterovesical junction obstruction/megaureter 5–15
Multicystic dysplastic kidney disease 2–5
Posterior urethral valves 1–5
Ureterocele, ectopic ureter, duplex system,urethral atresia, Prune belly syndrome, polycystic kidney diseases Uncommon
ETIOLOGY OF URINARY TRACT DILATION
DETECTED ON ANTENATAL ULTRASOUND2
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URINARY TRACT DILATION
UTD A2-3 (HIGH RISK)
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URINARY TRACT DILATION
UTD A2-3 (HIGH RISK)
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If other findings or risk factors are
present, the finding of UTD warrants
adjusting T21 risk and offering prenatal
testing
Likelihood ratio=1.3 for Trisomy 21
In a low risk population, UTDA1 is likely a
normal variant and doesn’t significantly
change aneuploidy risk.
URINARY TRACT DILATION AND
KARYOTYPE ABNORMALITIES
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URINARY TRACT DILATIONMANAGEMENT2
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URINARY TRACT OBSTRUCTION
Urethral obstruction
UVJ obstruction
Ureterocele
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URETERO-PELVIC JUNCTION (UPJ)
OBSTRUCTION-LONGITUDINAL
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URETERO-PELVIC JUNCTION (UPJ)
OBSTRUCTION-LONGITUDINAL
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URETERO-PELVIC JUNCTION (UPJ)
OBSTRUCTION-TRANSVERSE
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URETERO-VESICULAR JUNCTION (UVJ)
OBSTRUCTION
The
normal
fetal
ureter is
NEVER
visible!
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URETERO-VESICULAR JUNCTION (UVJ)
OBSTRUCTION
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URETEROCELE
(CAN CAUSE UVJ OBSTRUCTION)
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Fetal bladder fills and empties every 30-155 minutes
Fetal bladder wall not usually seen when normal
bladder is distended
FETAL BLADDER
PHYSIOLOGY/ANATOMY
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Etiology:
Posterior urethral
valves (Males)
Urethral atresia
Other: Megacystis-
microcolon, cloacal
malformations
Sonographic findings:
Bilateral UTD
Hydroureter
Distended bladder
Oligohydramnios
BLADDER OUTLET OBSTRUCTION
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“Keyhole Bladder”
BLADDER OUTLET OBSTRUCTION
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A. Transverse
UTDA2-3
B. Longitudinal
UTDA2-3 and
hydroureter
C. Transverse
thickened
bladder wall
D. “Keyhole sign”
and thickened
bladder wall
BLADDER OUTLET OBSTRUCTION
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Multicystic dysplastic kidneys
Cystic dysplasia
Autosomal recessive polycystic kidney disease (ARPKD)
Autosomal dominant (ADPKD)
CYSTIC KIDNEYS
In
utero
insult
Genetic
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Result of an EARLY (first trimester) urinary
tract obstruction
70-80% unilateral
Cysts vary in size
No communication between cysts, no
uniformity
Reniform contour is lost
Non-functioning kidney
25% of the time other anomalies are present
MULTICYSTIC DYSPLASTIC KIDNEY
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MULTICYSTIC DYSPLASTIC KIDNEY
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MULTICYSTIC DYSPLASTIC KIDNEY
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MULTICYSTIC DYSPLASTIC KIDNEY3
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BILATERAL MULTICYSTIC DYSPLASTIC
KIDNEYS3
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Result of a LATE (second/third trimester)
urinary tract obstruction
Common causes
UPJ obstruction
Bladder outlet obstruction
Results in irreversible renal damage
Usually few small cysts with a small,
echogenic kidney
CYSTIC DYSPLASIA
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CYSTIC DYSPLASIA3
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AUTOSOMAL RECESSIVE POLYCYSTIC
KIDNEY DISEASE
Autosomal recessive mutation of the PKHD1 gene,
locus 6p
Symmetric enlargement of both kidneys with
innumerable 1-2 mm cysts
+/- hepatic involvement
Typically diagnosable by 24 weeks but varies widely
and may not present until postnatal period
Sonographic findings
Progress with advancing gestational age
Loss of corticomedullary differentiation
Low amniotic fluid
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AUTOSOMAL RECESSIVE POLYCYSTIC
KIDNEY DISEASE-LONGITUDINAL
19 wks24 wks
32 wks38 wks
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AUTOSOMAL RECESSIVE POLYCYSTIC
KIDNEY DISEASE-TRANSVERSE
19 wks
32 wks
26 wks
36 wks
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85% due to PKD1 gene mutation on
chromsome 16.
Can also be due to PKD2 gene mutation
Severity of parental disease not predictive of
offspring disease
Cystic echogenic kidneys with NORMAL
amniotic fluid volume
Systemic disorder
Liver, pancreas, intracranial aneurysms, colonic
diverticulae
AUTOSOMAL DOMINANT POLYCYSTIC
KIDNEY DISEASE
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Difficult to differentiate from ARPKD
Assess family history
Get renal ultrasound on both parents
If normal, consider ARPKD
AUTOSOMAL DOMINANT POLYCYSTIC
KIDNEY DISEASE
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Differential Diagnosis (partial)
Normal variant
Cystic kidney disorders (previously discussed)
Bardet Biedl syndrome
Meckel Gruber syndrome
Trisomy 13 and 18
Beckwith-Wiedemann syndrome
ECHOGENIC KIDNEYS
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ECHOGENIC KIDNEYS
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Unilateral or bilateral
Bilateral renal agenesis
M:F ratio 2.5:1
100% mortality (?)
Sonographic findings
Oligo/anhydramnios
Bladder not visible
Kidneys not visible
Other anomalies common
ABSENT KIDNEYS
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UNILATERAL RENAL AGENESIS
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BILATERAL RENAL AGENESIS4
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BILATERAL RENAL AGENESIS4
“LYING DOWN ADRENAL” SIGN
Adrenal gland
Kidney
Normal
Adrenal gland
Renal agenesis
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BILATERAL RENAL AGENESIS5
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Upper pole
ureter
typically
implants
lower on the
bladder, and
is associated
with a
ureterocele
DUPLICATED COLLECTING SYSTEM
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DUPLICATED COLLECTING SYSTEM
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1. Quiroga, Hector. "Pelvic Kidney." Sonoworld . N.p., 02 June
2011. Web. 02 Apr. 2016.
2. Nguyen et al. Multidisciplinary consensus on the
classification of prenatal and postnatal urinary tract dilation
(UTD classification system). J Pediatr Urol 2014;10:982-
999.
3. Cullier, Fabrice . “Unilateral Multicystic Dysplastic Kidney."
Sonoworld . N.p., 09 Mar 2007. Web. 02 Apr. 2016.
4. Callen, Peter, MD. "Renal Agenesis." Renal Agenesis .
Ultrasound Educational Press, n.d. Web. 02 Apr. 2016.
5. Athale, Ajit . "Cochinblogs." : Sonography of Bilateral Renal
Agenesis in a Fetus: . N.p., n.d. Web. 02 Apr. 2016.
REFERENCES
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QUESTIONS?