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Placental pathology and antiphospholipid antibodies: a descriptive study
1Department of Pathology, Montefiore Medical Center, Bronx, New York, USA.
American Journal of Perinatology
|October 6, 1997
Summary
Antiphospholipid antibody (APL) syndrome can cause placental issues. Early miscarriages (<18 weeks) showed no APL-specific pathology, but later losses (18-22 weeks) revealed thromboses.
Area of Science:
- Obstetrics and Gynecology
- Pathology
- Immunology
Background:
- Antiphospholipid antibody (APL) syndrome is associated with adverse pregnancy outcomes.
- Understanding placental pathology is crucial for managing APL syndrome.
- Previous studies have not fully elucidated the spectrum of placental changes in APL syndrome across different clinical scenarios.
Purpose of the Study:
- To describe and compare placental pathology in antiphospholipid antibody (APL) syndrome.
- To investigate placental findings in treated and untreated APL syndrome pregnancies.
- To analyze placental pathology in relation to recurrent pregnancy loss and serological APL.
Main Methods:
- Histopathological review of 39 placentas from 28 patients with APL.
- Inclusion of placentas from pregnancies with APL syndrome, serological APL, and prior miscarriages.
- Blinded histopathological assessment by a pathologist, with statistical analysis using contingency tables and ANOVA.
Main Results:
- Placentas from treated APL syndrome pregnancies showed a trend towards more perivillous coagulation, avascular villi, and vasculitis compared to serological APL (p=0.07).
- Miscarriages before APL diagnosis (<18 weeks) lacked APL-typical pathology, though chronic intervillositis was noted in 36%.
- Multifocal uteroplacental thromboses occurred in 60% of miscarriages after 18 weeks, compared to 46% in treated APL syndrome and 0% in serological APL.
Conclusions:
- Placental pathology in APL syndrome varies with treatment status and gestational age at loss.
- Uteroplacental thromboses are a significant finding in later miscarriages and treated APL syndrome pregnancies.
- Further research is needed to refine diagnostic criteria and therapeutic strategies for APL-associated pregnancy complications.