The study found a high prevalence of mutations associated with clonal hematopoiesis in patients with Erdheim-Chester disease, shedding light on the molecular mechanisms of ECD and its known association with other myeloid neoplasms.
In this issue of Blood, Cohen Aubart et al report a high prevalence (42.5%) of mutations associated with clonal hematopoiesis (CH) in bone marrow specimens of patients with Erdheim-Chester disease (ECD).(1) These novel findings shed light upon the molecular underpinnings of ECD and its well-known association with other myeloid neoplasms.
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