ArticleCureus2026
Focal Cerebral Arteriopathy in a Young Adult.
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.
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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Focal cerebral arteriopathy (FCA) is a rare, monophasic stenosis of the distal internal carotid artery (ICA) or proximal middle cerebral artery that primarily affects children but is occasionally seen in adults. It is unclear what causes FCA in adults, which complicates diagnosis and management. The case presented highlights diagnostic challenges using multimodal imaging, supporting conservative management, and the need for adult-specific treatment criteria. A 38-year-old woman with a history of breast cancer, migraines, and prior pulmonary embolism presented with a sudden-onset thunderclap headache and expressive aphasia. Initial imaging revealed high-grade left ICA terminus stenosis, with differential diagnoses including reversible cerebral vasoconstriction syndrome and vasculitis. The patient was readmitted two days after her initial presentation for worsening symptoms, including right-sided facial and arm numbness, as well as visual hallucinations. Multimodal imaging, blood work, and lumbar puncture excluded alternative diagnoses. Digital subtraction angiography confirmed 70% left supraclinoid ICA stenosis that was unresponsive to intra-arterial verapamil, ruling out reversible cerebral vasoconstriction syndrome. Serial imaging demonstrated progressive improvement in the stenosis (59% at one month and 46% at six months). The patient has not experienced symptom recurrence and reports being at her neurologic baseline. This case underscores the challenges of diagnosing FCA in young adults because of its overlap with several other arteriopathies, resulting in unnecessary interventions and lifelong misdiagnosis. Multimodal imaging is critical for accurate diagnosis and monitoring. The self-limiting nature of FCA supports conservative management, but adult-specific diagnostic criteria are needed to improve recognition and guide therapy.
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.