A Rare Coexistence of Multiple Myeloma and Polycythemia Vera.

IF 1.3 Q4 HEMATOLOGY Journal of hematology Pub Date : 2023-10-01 Epub Date: 2023-10-21 DOI:10.14740/jh1167
Alexander Landsman, Priyanka Barua, Alida Podrumar
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Abstract

Multiple myeloma (MM) is classically associated with organ dysfunction leading to hypercalcemia, renal insufficiency, anemia and bone disease, known as the CRAB criteria. More than 70% of patients with MM present with anemia. Few rare case reports, however, have demonstrated the presentation of MM associated with polycythemia. We present an interesting case of a 65-year-old female who was initially diagnosed with monoclonal gammopathy of undetermined significance (MGUS) which progressed to smoldering myeloma and later developed into MM. The patient also had coexisting polycythemia vera (PCV). We discuss the typical patient presentations as well as the expanded diagnostic criteria for MM. The pathophysiology explaining the coexistence of polycythemia and MM will be explored as well.

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罕见多发性骨髓瘤和维拉红细胞增多症并存。
多发性骨髓瘤(MM)通常与导致高钙血症、肾功能不全、贫血和骨病的器官功能障碍有关,被称为CRAB标准。超过70%的MM患者表现为贫血。然而,很少有罕见病例报告显示MM与红细胞增多症相关。我们报告了一个有趣的病例,一名65岁的女性,最初被诊断为意义不明的单克隆gammopathy(MGUS),发展为闷烧性骨髓瘤,后来发展为MM。该患者还患有共存的真性红细胞增多症(PCV)。我们讨论了MM的典型患者表现以及扩展的诊断标准。解释红细胞增多症和MM共存的病理生理学也将进行探讨。
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Journal of hematology
Journal of hematology HEMATOLOGY-
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