- Fetal Upturned Nose
- IgA Nephropathy in Pregnancy
- Umbilical vein varix
- Timing of Cranial Markers in Open NTD
- Real world experience Open Neural tube defect and Brain Signs
- Real world experience First Trimester Megacystis – Management
- Real world experience Fetal Megacystis
- Abnormal facial profile
- Azygous Vein & ARSA
- Blakes Pouch Cyst
- Absent nasal bone (ANB)
- Choroid plexus cysts
- Chronic placental abruption
- Fetal Alcohol Syndrome
- Placenta-First Risk Stratification
- AVSD
- Blakes Pouch Cyst
- Confined Placental Mosaicism
- Echogenic Bowel
- Fetal Anemia
- Fetal Club Foot
- Fetal Mild Micromelia
- Hypochondroplasia – Mild Micromelia
- Hypoplastic Nasal Bone
- IgM IgG IgG Avidity
- Increased Nuchal Translucency
- Isotretinoin in Pregnancy
- Partial agenesis of corpus callosum
- PGT A
- PGT-A Mosaicism to CPM
- Placenta First - CPM
- Radiation exposure during pregnancy
- Real world Chorionic bump experience
- Real world Fetal Isotretinoin exposure
- Real world Increased Nuchal Translucency & Genetic RISK
- Real world Renal Pyelectasis
- Real world Transient NT & Cystic Hygroma
- Real world Transient NT
- Renal Pyelectasis or Extra Renal Pelvis
- Right And Double Aortic Arch
- Short Femur Length Foot FL ratio
- Y Microdeletion
- CCAM CPAM
- Coffin–Siris syndrome
- Congenital CMV Infection
- Increased NT and Localized CHAOS
- Indomethacin and Reduction for AFI
- Atrioventricular septal defect (AVSD)
- Choledochal cyst & Cystic biliary atresia
- Duodenal Atresia
- Fetal atrial bigeminy
- Fetal Dilated stomach
- Mutation Types in DMD
- Risk of rubella in nonimmune pregnant woman
- Salt-losing nephropathy
- Syndromic Cystic biliary atresia
- TGA DORV TOF CCTGA
- Unilateral echogenic kidney with polyhydramnios
- Unilateral renal agenesis, Ectopic, Cross fused kidney
Real world Mild Renal Pyelectaiss
Measure anteroposterior renal pelvic diameter (APRPD) in transverse plane.
Second trimester (16–28 weeks)
- 4–6 mm → Mild
- 7–10 mm → Moderate
- >10 mm → Severe (hydronephrosis)
Third trimester
- 7–9 mm → Mild
- 10–15 mm → Moderate
- >15 mm → Severe
Bilateral mild pyelectasis in the second trimester is common and often benign.
Male fetuses
Much more common.
Reasons:
- Physiologic dilation
- Higher rate of vesicoureteral reflux (VUR)
- Posterior urethral valves (if severe and progressive)
If mild and isolated in a male fetus → usually benign.
Female fetuses
Less common.
Reasons:
- Reflux
- Less commonly obstruction
- Slightly higher suspicion threshold than in males
Resolution patterns
Mild (4–6 mm at 20 weeks)
- ~70–80% resolve antenatally or in early infancy
- Higher resolution rate in males
Moderate
- 40–60% resolve
- Some persist but remain clinically insignificant
Severe
- Low spontaneous resolution
- Higher postnatal pathology rate
If bilateral mild pyelectasis improves or stabilizes by 28–32 weeks → very reassuring.
Red flags
- Progressive dilation
- Renal pelvic diameter >10 mm in 2nd trimester
- Calyceal dilation
- Cortical thinning
- Oligohydramnios
- Dilated ureters
- Thick-walled bladder
- Associated anomalies
- Soft markers for aneuploidy
Aneuploidy risk
Isolated mild pyelectasis is a soft marker for Trisomy 21
- Risk increase is small
- Much lower if NIPT is low risk
- Much lower if no other markers
If truly isolated and NIPT low risk → no invasive testing required.
Amniocentesis if
- Bilateral moderate or severe dilation
- Additional soft markers
- Structural anomalies elsewhere
- Abnormal NIPT
- Progressive worsening
- Oligohydramnios suggesting obstruction
Invasive testing NOT recommended
- Mild (4–6 mm)
- Isolated
- Low-risk NIPT
- Normal anatomy
- Normal fluid
- Stable or improving
Postnatal prognosis
Isolated mild bilateral pyelectasis
- Excellent prognosis
- Most normalize
- Small percentage have low-grade reflux
- Rare need for surgery
Moderate persistent
- Postnatal ultrasound at 48–72 hours
- Repeat at 4–6 weeks
- Some may need VCUG
- Surgery uncommon unless obstruction
Severe bilateral with obstruction
Risk of:
- Posterior urethral valves (male)
- Bilateral UPJ obstruction
- Renal impairment
Prognosis depends on:
- Amniotic fluid
- Cortical thickness
- Postnatal renal function
If it is:
- Bilateral
- Mild
- Normal AFI
- Normal parenchyma
- NIPT low risk
That is usually a benign variant with high likelihood of resolution.
If:
- Bilateral moderate/severe
- Progressive
- Additional findings
For mild isolated bilateral pyelectasis:
“This is a common finding, especially in male fetuses. In most cases it resolves before or shortly after birth. At present there are no signs of kidney damage or obstruction.”