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E-cadherin/CD34 double immunostaining in placental diagnosis
1Division of Pathology, Cincinnati Children's Hospital, Cincinnati, United States.
Summary
A novel double immunostain using E-cadherin and CD34 effectively identifies placental foetal vascular malperfusion (FVM) and its temporal patterns. This method aids in diagnosing fetal death and poor neonatal outcomes, improving placental pathology assessments.
Area of Science:
- Pathology
- Perinatal Medicine
- Immunohistochemistry
Background:
- Placental foetal vascular malperfusion (FVM) is linked to adverse fetal and neonatal outcomes.
- Standard histological stains like H&E may not reveal subtle signs of recent FVM.
Purpose of the Study:
- To evaluate the utility of a double E-cadherin/CD34 immunostain in diagnosing FVM and other placental pathologies.
- To assess the stain's ability to identify recent FVM, temporal heterogeneity, and differentiate specific placental lesions.
Main Methods:
- Routine application of a double E-cadherin/CD34 immunostain on placental sections, particularly from complicated pregnancies.
- Analysis of endothelial fragmentation, basement membrane changes, and differentiation of mineralized thrombi versus pseudo-inclusions.
Main Results:
- The double immunostain highlights distal villous endothelial fragmentation indicative of recent FVM, often missed by H&E.
- It reveals temporal heterogeneity of FVM, aiding in determining causes of fetal death or poor neonatal condition.
- The stain assists in diagnosing distal villous hypomaturity, differentiates mineralized stem occluding thrombi from pseudo-inclusions, and aids in identifying trophoblastic lesions in shallow placental implantation.
Conclusions:
- The double E-cadherin/CD34 immunostain is a valuable tool for the histological diagnosis of placental lesions and patterns of injury.
- It enhances the detection and characterization of FVM, contributing to improved understanding of fetal and neonatal complications.
- This technique offers diagnostic advantages in differentiating FVM from placental aneuploidies and assessing trophoblastic lesions.

