继发性多血细胞症可能是多发性骨髓瘤的早期临床表现:病例报告

IF 2.1 Q3 HEMATOLOGY Journal of Blood Medicine Pub Date : 2024-07-29 eCollection Date: 2024-01-01 DOI:10.2147/JBM.S465827
XiaoLan Li, Min Li, Juan Tian, Zi-Wei Shi, Ling-Zhi Wang, Kui Song
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引用次数: 0

摘要

多发性骨髓瘤(MM)是一种浆细胞恶性肿瘤,可因肾功能衰竭和骨髓衰竭而导致贫血。继发性多血细胞症(SE)是一种临床罕见的红细胞生成过多的疾病。据我们所知,多发性骨髓瘤与多血症的关联已有报道,但继发性多血症与多发性骨髓瘤的关联并不多见,文献中也鲜有报道。与贫血不同,多发性骨髓瘤患者出现多血细胞症是一个罕见的发现。现将我科最近收治的一名继发性红细胞增多症的IgA-λ多发性骨髓瘤患者报告如下,并回顾相关文献,以提高临床医生对此类罕见合并症的认识。
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Secondary Polycythemia May Be an Early Clinical Manifestation of Multiple Myeloma: A Case Report.

Multiple myeloma (MM) is a malignancy of plasma cells that can cause anemia due to renal failure and bone marrow failure. Secondary polycythemia (SE) is a clinically rare disease that involves the overproduction of red blood cells. To our knowledge, the association of multiple myeloma and polycythemia has been reported, but the association of SE and multiple myeloma is rare and has been infrequently reported in literature. In contrast to anemia, the presence of polycythemia in multiple myeloma patients is a rare finding. A patient of IgA-λ multiple myeloma with secondary erythrocytosis recently admitted to our department is now reported as follows and relevant literature is reviewed to improve clinicians' awareness of such rare comorbidities.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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