Evidence map›Paper›PMID 42694317›Full record

ArticleCureus2026

Late-Onset Antiphospholipid Syndrome Presenting With Recurrent Multifocal Ischemic Strokes: Diagnostic and Management Challenges.

Mariam Ahmed, Mohamed A Ahmed, William Boadu

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Mariam AhmedMedicine, Qatar University, Doha, QAT.
Mohamed A AhmedAnatomical Sciences, St. George's University School of Medicine, St. George's, GRD.
William BoaduNeurology, Mater Olbia Hospital, Olbia, ITA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiphospholipid syndrome (APS) is an autoimmune prothrombotic disorder that predominantly affects women of childbearing age and is a recognized cause of ischemic stroke. In older adults, APS is uncommon and frequently overlooked because cerebrovascular events are often attributed to traditional vascular risk factors, resulting in delayed diagnosis and treatment. We report the case of a 65-year-old woman with a history of hypertension, dyslipidemia, chronic kidney disease, recurrent transient ischemic attacks (TIAs), previous intraventricular hemorrhage, and intracranial aneurysm repair, who presented with dysarthria, gait ataxia, and quadriparesis. She had experienced multiple recurrent cerebrovascular events over several years despite extensive vascular and cardiac investigations and appropriate antiplatelet therapy. Brain magnetic resonance imaging (MRI) demonstrated multiple acute multifocal ischemic infarcts involving both cerebral hemispheres on a background of extensive chronic ischemic changes. Laboratory evaluation revealed mild thrombocytopenia and a high-risk antiphospholipid antibody (aPL) profile, including positive lupus anticoagulant (LA) and markedly elevated anti-β2-glycoprotein I (β2GPI) IgG antibodies, while anticardiolipin (aCL) IgG and IgM antibodies were negative. As APS classification criteria require persistent aPL positivity on repeat testing at least 12 weeks apart, initiation of long-term anticoagulation was deferred pending confirmatory testing. This decision was further influenced by the patient's increased bleeding risk due to previous intracranial hemorrhage. Aspirin therapy continued while she underwent rehabilitation and awaited repeat antibody testing. This case highlights the diagnostic and therapeutic challenges of elderly-onset APS presenting with recurrent multifocal ischemic strokes. APS should be considered in older patients with recurrent or unexplained ischemic strokes, particularly when routine vascular and cardiac evaluations do not identify an adequate cause. Early recognition and appropriate serological testing may reduce diagnostic delays and facilitate secondary stroke prevention. Management requires individualized risk-benefit assessment, especially when anticoagulation is considered in patients with significant bleeding risk.

Indexed as

antiphospholipid antibodyantiphospholipid syndromehypercoagulabilityischemic strokethromboembolic event

Identifiers

PMID42694317
PMCPMC13539016

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