Fetal Anemia
Karen Y. Oh, MD
DIFFERENTIAL DIAGNOSIS
Common
Alloimmunization
Rh Incompatibility
Other Antibodies
Infection
Parvovirus B19
Rare but Important
Hemangioendothelioma
Leukemia
Fanconi Anemia
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Clinical history is often key to diagnosis
Watch for fetal anemia with maternal history of isoimmunization
Usually with Rh negative maternal blood types
Can have other minor antibody sensitizations
Obtain history of potential viral exposures
Look for associated fetal abnormalities which can cause fetal anemia
Tumors
Vascular malformations
Always consider anemia when a fetus presents with hydrops
Middle cerebral artery (MCA) Doppler peak systolic velocity (PSV) measurements elevated in anemia
Very accurate noninvasive method to screen for fetal anemia
Helpful Clues for Common Diagnoses
Rh Incompatibility
Occurs in women who are Rh (-)
Indicates absence of D antigen in erythrocyte membrane
Results from maternal immune response against RhD antigen on fetal red blood cells
Maternal anti-D antibodies cross placenta
Leads to lysis of fetal erythrocytes
Prophylaxis should be given routinely if woman is Rh (-) and when fetal and maternal blood could be in contact
Ectopic pregnancy
Post chorionic villus sampling or amniocentesis
Following spontaneous or elective abortion
Maternal trauma
At time of delivery of an Rh + infant
Prophylactic dose given at approximately 28 weeks gestation
If no prior history of antibody sensitization → correlate with antibody titers to assess for risk of fetal anemia
If history of prior sensitization → plan for increased surveillance and monthly antibody titer until critical titer reached (generally 1:8-1:16)
Once critical titer reached, then follow serial MCA-PSV
Fetal hemolytic disease similar to or more severe in subsequent pregnancies
Serial ultrasound evaluation
Monitor for hydrops
Check PSV in MCA
Increased PSV indicates worsening fetal anemia
Follow-up interval and intervention based on PSV measurements compared to normative scale (Mari zones A-D)
Cordocentesis and transfusion if anemia severe
Other Antibodies
Most sensitizations caused by incompatible blood transfusions
Includes Kell, Duffy, Kidd, E, C, c and multiple other antigens
Similar management of pregnancy as with Rh alloimmunization
Parvovirus B19
20-30% of women who become infected during pregnancy transmit to fetus
4% risk of fetal hydrops
Highest risk of fetal death if infected < 20 wks gestation
Fetal anemia causes sonographic findings
Parvovirus attacks red blood cell precursors
Involvement of cardiac myocytes may contribute to hydrops
Ascites most common presenting finding
Progression to hydrops in severe cases
Maternal infection should be managed by high risk specialist
Weekly ultrasound for 10-12 weeks after seroconversion
Check for developing hydrops
Monitor MCA Doppler PSV to assess for fetal anemia
Intrauterine transfusion warranted for fetal anemia
Helpful Clues for Rare Diagnoses
Hemangioendothelioma
Typically solid, well-defined large mass
Variable echogenicity: Can be hypoechoic, hyperechoic or mixed echogenicity
Very vascular mass with arteriovenous shunting on color Doppler
Arteriovenous shunting may result in hemolytic anemia (Kasabach-Merritt sequence)
Both vascular shunting and anemia contribute to development of hydrops
Leukemia
Usually presents with hepatosplenomegaly
Unlike other liver tumors, most commonly diffuse enlargement rather than focal mass
Associated with Down syndrome
Hydrops can develop due to multiple factors
Fetal anemia
Leukemic infiltration of myocardium
Visceral fibrosis with increased vascular resistance
Fanconi Anemia
Inherited bone marrow failure syndrome
Autosomal recessive
Multiple known gene mutationsStay updated, free articles. Join our Telegram channel
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