Coexistence of Essential Thrombocythemia and Waldenström Macroglobulinemia: A Case Report.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-08-28 eCollection Date: 2025-01-01 DOI:10.1155/crh/3390770
Meghan Wallace, Bruce Mathey, Cecilia C S Yeung, Jacob S Appelbaum, Mark Wallace
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引用次数: 0

Abstract

Waldenström macroglobulinemia (WM) and essential thrombocythemia (ET) are distinct hematologic malignancies that have only been reported to co-occur in one previous patient. We present a 64-year-old man with a significant family history for WM who was found to have both ET and WM. He had symptomatic ET, diagnosed by elevated platelets and a positive JAK2 V617F mutation, and asymptomatic WM was found on serum electrophoresis done for screening due to family history. Genomic evaluation of the myeloid and lymphoid cells suggested independent neoplastic transformation. This is the second reported case of a patient with both WM and ET. There was no evidence for a shared mechanism in these dual malignancies.

Abstract Image

原发性血小板增多症和Waldenström巨球蛋白血症共存1例报告。
Waldenström巨球蛋白血症(WM)和原发性血小板血症(ET)是不同的血液系统恶性肿瘤,仅报道在既往患者中同时发生。我们报告一位64岁的男性,有明显的WM家族史,被发现同时患有ET和WM。他有症状性ET,通过血小板升高和JAK2 V617F阳性突变诊断,由于家族史,筛查时血清电泳发现无症状性WM。髓细胞和淋巴细胞的基因组评估提示独立的肿瘤转化。这是报道的第二例同时患有WM和ET的病例。没有证据表明这两种恶性肿瘤有共同的机制。
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审稿时长
13 weeks
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