Gat Roi, Trestman Svetlana, Kirgner Ilya
Department of Hematology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Acta Haematol. 2025 Mar 29:1-5. doi: 10.1159/000545479.
Acquired factor X (FX) deficiency is a rare coagulopathy. Occurrences in plasma cell dyscrasias (PCDs) independent of amyloid light-chain amyloidosis are exceedingly rare.
This case report presents a rare occurrence of acquired FX deficiency in a patient with multiple myeloma (MM) without concomitant amyloidosis. The patient, a 64-year-old male with prior diagnosis of smoldering MM, presented with abdominal pain and chronic bloody diarrheas and was diagnosed with absolute FX deficiency. Despite initial suspicion of amyloidosis, subsequent investigations ruled out its presence. Treatment with anti-myeloma therapy and supportive measures resulted in the normalization of coagulation parameters.
This case underscores the importance of considering acquired FX deficiency in PCD patients presenting with coagulopathy even in the absence of amyloidosis.
获得性因子X(FX)缺乏是一种罕见的凝血病。在独立于淀粉样轻链淀粉样变性的浆细胞异常增生症(PCD)中出现极为罕见。
本病例报告呈现了1例罕见的在无淀粉样变性的多发性骨髓瘤(MM)患者中发生获得性FX缺乏的情况。该患者为一名64岁男性,既往诊断为冒烟型MM,出现腹痛和慢性血性腹泻,被诊断为绝对FX缺乏。尽管最初怀疑为淀粉样变性,但后续检查排除了其存在。采用抗骨髓瘤治疗和支持措施后凝血参数恢复正常。
本病例强调即使在无淀粉样变性的情况下,对于出现凝血病的PCD患者也需考虑获得性FX缺乏。