Idiopathic erythrocytosis: A diagnostic and management challenge with emerging areas for exploration

Abstract

SummaryDespite published algorithms for approaching the work‐up of erythrocytosis, a significant proportion of patients are left with uncertainty as to its aetiology and prognosis. The term ‘idiopathic erythrocytosis’ (IE) is applied when known primary and secondary aetiologies have been ruled out. However, the assignment of secondary aetiologies is not always straightforward or evidence based, which can lead to misdiagnosis and heterogeneity in cohort studies. Furthermore, new studies have identified germline or somatic mutations that may affect prognosis. Epidemiological and cohort data are inconsistent as to whether IE increases the risk for complications such as arterial and venous thromboembolism, clonal transformation or comorbid conditions. Randomized trials assessing the role of phlebotomy for long‐term management of IE have not been performed, so treatment remains a vexing problem for clinicians. Standardization of terminology and testing strategies, including comprehensive genetic screening in clinical research, are key to refining our understanding of IE.