ArticleWorld journal of clinical cases2023
Cerebral proliferative angiopathy in pediatric age presenting as neurological disorders: A case report.
Article in World journal of clinical cases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
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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.
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Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.
- Presentation and management of cerebral proliferative angiopathy: a systematic review and meta-analysis on treatment outcomes.Neurosurgical review · 2024Pooled it
- Cerebral proliferative angiopathy in pediatric patients: case-based review with an illustrative case.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026Review
- Encephaloduroarteriomyosynangiosis with the middle meningeal artery for proliferative cerebral angiopathy treatment: A case report.Surgical neurology international · 2025Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundCerebral proliferative angiopathy (CPA) is a rare subtype of arteriovenous malformation. It is extremely rare in pediatric patients and has serious implications for developing children. However, reports of these disorders worldwide are limited, and no uniform reference for diagnosis and treatment options exists. We report the case of a 6-year-old with CPA having predominantly neurological dysfunction and review the literature on pediatric CPA. CASE SUMMARY: We report the case of a pediatric patient with CPA analyzed using digital subtraction angiography (DSA) who presented initially with a neurological disorder as the main manifestation. This case is the basis for further discussion of the clinical presentation, pathogenesis, diagnosis, and treatment of CPA in children. After the cerebral DSA, the patient was treated conservatively with sedation, fluid replacement, and blood anticoagulation. She could not cooperate with the follow-up magnetic resonance imaging examination because of her young age, and her family declined further treatment because of the surgery's high risk. She was followed up for 3 months; her symptoms did not worsen.
conclusionThis report of rare pediatric CPA can inform and advance clinical research on congenital cerebrovascular diseases.
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Registered trials
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