Polyhydramnios
Roya Sohaey, MD
DIFFERENTIAL DIAGNOSIS
Common
Idiopathic
Macrosomia
Diabetes
Hydrops
Twin-Twin Transfusion Syndrome
Fetal Bowel Obstruction
Less Common
Arthrogryposis, Akinesia Sequence
Skeletal Dysplasia, Severe
Chorioangioma
Cystic Adenomatoid Malformation
Rare but Important
Mesoblastic Nephroma
Unilateral Ureteropelvic Junction Obstruction
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Amniotic fluid index (AFI)
Divide uterus into 4 equal quadrants
Measure maximum vertical pocket (MVP)
Avoid fetal parts/cord in MVP
Add the 4 MVPs to calculate AFI
AFI/gestational age normogram tables available
> 24 cm AFI = polyhydramnios
Twin fluid assessment
Measure MVP for each fetus
≥ 8 cm = polyhydramnios
Helpful Clues for Common Diagnoses
Idiopathic
Most common cause (2/3)
Mild, stable finding
Normal patient and fetus
No diabetes or fetal anomalies
28% with fetal macrosomia
Macrosomia
Estimated fetal weight > 90th percentile
Large abdominal circumference is a hallmark finding
↑ Truncal echogenic fat
Causes
Hereditary characteristics
Maternal obesity
Diabetes
Beckwith-Wiedemann syndrome
Diabetes
Gestational diabetes (most common)
Glucose intolerance during pregnancy
Oral glucose tolerance test given between 24-28 wks
Pregestational diabetes (type 1 or 2)
Polyhydramnios associated with poor glucose control
May be first finding in pregnancy
Associated with macrosomia
Hydrops
Excessive fetal fluid accumulation (2 or more body cavities)
Anasarca
Pleural effusion (± pericardial)
Ascites
Amniotic fluid may be ↑ or ↓
Immune hydrops (10%)
Non-immune (90%)
Infection
Any cause of fetal anemia
Any cause of fetal heart failure
Lymphatic obstruction
Aneuploidy associations
Turner syndrome (cystic hygroma)
Trisomy 21
Trisomy 18
Twin-Twin Transfusion Syndrome
Monochorionic twinning
Artery-to-vein anastomoses in shared placenta
Donor twin partly perfuses recipient twin
Fluid discrepancy may be 1st sign of developing twin-twin transfusion syndrome (need to follow carefully)
Recipient twin with polyhydramnios
Larger twin
Donor twin with oligohydramnios
Smaller “stuck” twin
Fetal Bowel Obstruction
Late polyhydramnios (> 24 wks)
Esophageal atresia
Absent or small stomach
1/3 with trisomy 18 or 21
Associated with VACTERL syndrome
Duodenal atresia
“Double-bubble” appearance
1/3 with trisomy 21
Jejunal, ileal atresia
“Sausage-shaped” bowel loops
Helpful Clues for Less Common Diagnoses
Arthrogryposis, Akinesia Sequence
Heterogeneous group of disorders
Lack of extremity motion
Contractures
Polyhydramnios from ↓ fetal movement/swallowing
Associations
Trisomy 18
Autosomal dominant and recessive syndromes
Skeletal Dysplasia, Severe
Common dysplasias
Thanatophoric
Achondroplasia
Achondrogenesis
Osteogenesis imperfecta
Common skeletal findings
Short limbs
Poor ossification
Bowed or broken bones
Craniosynostosis
Polyhydramnios common in 3rd trimester
Chorioangioma
Benign, vascular placental tumor
Large masses (> 5 cm): ↑ Complications
Polyhydramnios
Transudate from leaky vessels
Hydrops
Arteriovenous shunting in mass
Fetal anemia from hemolysis
Cystic Adenomatoid Malformation
Lung hamartoma
Microcystic and macrocystic types
Polyhydramnios etiology
Esophagus compression
Associated with hydrops
Mass may make fluid
Helpful Clues for Rare Diagnoses