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Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report | Synapse
March 3, 2026
Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report
AA
Abdullah Abdulrahman AlShamrani
AA
Ali Muhammad Alqaraishi
AA
Ahmed Saad Almukhlifi
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Key Points
Coronary vasospasm was observed, leading to significant cardiac implications for the patient.
The case highlights the association between RUNX1 mutation and eosinophilic leukemia, emphasizing its role as a potential biomarker.
The patient exhibited pronounced symptoms from hypereosinophilic syndrome, reflecting systemic involvement.
This case underscores the need for careful cardiovascular assessment in patients with genetic mutations related to blood disorders.
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AlShamrani et al. (Thu,) studied this question.
synapsesocial.com/papers/69a75b37c6e9836116a22270
https://doi.org/https://doi.org/10.1016/j.jccase.2026.01.001