Evidence map›Paper›PMID 41994071›Full record

ArticleJournal of cardiology cases2026

Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report.

Abdullah Abdulrahman AlShamrani, Ali Muhammad Alqaraishi, Ahmed Saad Almukhlifi, Aeshah M Alharbi, Rashed S Alharbi, Rajkumar Rajendram

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In one paragraph

Article in Journal of cardiology cases, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Abdullah Abdulrahman AlShamraniThe Department of Medicine, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Ali Muhammad AlqaraishiThe Department of Medicine, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Ahmed Saad AlmukhlifiThe Department of Medicine, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Aeshah M AlharbiThe Department of Medicine, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Rashed S AlharbiDepartment of Family Medicine, King Fahad Medical City, Riyadh, Saudi Arabia.
Rajkumar RajendramResearch Offices, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypereosinophilic syndrome (HES) is characterized by persistent eosinophilia and the potential for significant organ damage. Cardiac involvement, a frequent complication, may be life-threatening. We describe the case of a 29-year-old male who presented with chest pain and dyspnea and was found to have eosinophilia. A comprehensive workup, including extensive laboratory and imaging studies, bone marrow aspirate and trephine with cytogenetic testing failed to identify a cause for the HES. Thus, the patient was provisionally diagnosed with idiopathic HES and treated with steroids. Although cytogenetic chromosomal analysis and fluorescence in situ hybridization for myeloid genes were negative, next generation sequencing (NGS) revealed a likely pathogenic variant in RUNX1 consistent with myeloid leukemia. RUNX1 also regulates adverse cardiac remodeling after myocardial infarction. Thus, this case highlights the importance of thorough investigation to determine the etiology of HES and the need to define the role of RUNX1 mutations. Early recognition and prompt initiation of appropriate therapy is crucial for mitigating organ damage and improving patient outcomes. When the diagnosis is uncertain, corticosteroids can be used to control eosinophilia which may be lifesaving. Yet, this case underscores the importance of a comprehensive diagnostic approach, including NGS, in patients with unexplained eosinophilia and cardiac involvement. Learning objectives: Hypereosinophilic syndrome should be considered in patients with unexplained eosinophilia and systemic symptoms.Eosinophilic myocarditis may mimic acute coronary syndromes and can coexist with coronary vasospasm.Early corticosteroid therapy can prevent irreversible organ damage. Comprehensive evaluation is necessary to exclude secondary causes of eosinophilia.Detection of somatic mutations such as RUNX1 may indicate an underlying clonal eosinophilic disorder and warrants hematology input and long-term monitoring.Multidisciplinary care, including cardiology and hematology input, is vital for optimal management.

Indexed as

Coronary vasospasmEosinophilic leukemiaHypereosinophilic syndromeIdiopathic hypereosinophilic syndromeMyocardial infarctionRUNX1 mutation

Identifiers

PMID41994071
PMCPMC13081061

What Socratic holds

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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 Socratic graph.