ArticleFrontiers in immunology2025
Case Report: The case of atypical OAPS complicated by positive anti-SSA and anti-SSB antibodies.
Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Antiphospholipid syndrome (APS) is a systemic autoimmune disease. When pathological pregnancy manifestations-such as recurrent miscarriage, stillbirth, preeclampsia, and preterm birth-predominate, the condition is called obstetric APS (OAPS). OAPS can be typical or atypical. Pregnant women positive for anti-Ro/SSA and SSB antibodies may develop fetal congenital heart block (CHB). Meanwhile, antiphospholipid antibodies (aPL) can cause preeclampsia, fetal growth restriction, intrauterine fetal death, and other adverse outcomes through mechanisms including disruption of trophoblast function. Here, we describe a case of atypical OAPS complicated with anti-Ro/SSA and SSB antibody positivity during pregnancy, who developed a subchorionic hematoma. At presentation, the hematoma was progressively enlarging, yet the patient had only one moderate-to-high titer of anti-β2-GP1 antibody and a transient low titer of ACL-IgM, not meeting clinical or laboratory criteria for OAPS. Delaying diagnosis and treatment to wait for repeat aPL testing after 12 weeks would increase risk of poor outcomes. Facing overtreatment and undertreatment challenges, we chose high-dose corticosteroids, hydroxychloroquine, and intravenous immunoglobulin therapy. When the hematoma shrank, low-molecular-weight heparin (LMWH) and aspirin were added with close monitoring, and after two weeks, both the hematoma and placental blood sinuses resolved. During pregnancy follow-up, multiple anti-β2-GP1 antibody tests showed moderate-to-high titers (over 12 weeks apart), confirming our diagnosis. Besides these immunological abnormalities, the patient was also positive for anti-SSA and anti-SSB antibodies and had a prior pregnancy complicated by suspected fetal ventricular septal defect, a high-risk factor. In light of this risk, the patient was treated with hydroxychloroquine. As a preventive strategy, two courses of intravenous immunoglobulin (IVIG) were also initiated at 16 weeks of gestation to support maternal-fetal immune tolerance. After treatment, no fetal cardiac abnormalities were observed, and a healthy female infant was vaginally delivered at 38 + 4 weeks. Diagnosing such cases and correct timing and choice of medication are critical for women of childbearing age. Most women with immune-related antibody positivity can achieve successful pregnancy and delivery with appropriate treatment.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.