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获得性因子 X 缺乏症合并多发性骨髓瘤而不伴淀粉样变性:一例报告。

Acquired factor X deficiency in a multiple myeloma without amyloidosis: a case report.

机构信息

Department of Laboratory Medicine, AZ Damiaan, Oostende, Belgium.

Department of Laboratory Medicine, AZ Sint-Jan, Brugge, Belgium.

出版信息

Acta Clin Belg. 2023 Dec;78(6):524-528. doi: 10.1080/17843286.2023.2265650. Epub 2023 Oct 16.

DOI:10.1080/17843286.2023.2265650
PMID:37800976
Abstract

BACKGROUND

Multiple myeloma is one of the most common hematologic malignancies. Acquired factor X deficiencies are often observed in primary (AL) amyloidosis and rarely in multiple myeloma.

OBJECTIVE

We report a case of an acquired factor X deficiency in a patient with a newly diagnosed IgA lambda multiple myeloma, without any evidence of concomitant amyloidosis.

METHODS

We present the patient's medical history, clinical and physical examinations, laboratory analysis, and outcome.

RESULTS

A 76-year-old male presented at the emergency department with ongoing gingival bleeding. Several analytical problems with blood sample analysis arose, which eventually led to the diagnosis of a multiple myeloma. Further exploration revealed an acquired factor X deficiency, explaining the ongoing bleeding. There was no evidence of concomitant amyloidosis. The multiple myeloma was treated, leading to complete remission of the malignancy and bleeding tendency.

CONCLUSION

While coagulopathy is rarely observed in patients diagnosed with multiple myeloma, considering an acquired factor X deficiency becomes relevant when such patient present with bleeding diathesis.

摘要

背景

多发性骨髓瘤是最常见的血液系统恶性肿瘤之一。获得性因子 X 缺乏症在原发性(AL)淀粉样变性中经常观察到,在多发性骨髓瘤中很少见。

目的

我们报告了一例新诊断的 IgA λ 型多发性骨髓瘤患者中出现获得性因子 X 缺乏症的病例,无同时存在淀粉样变性的证据。

方法

我们介绍了患者的病史、临床和体格检查、实验室分析和结果。

结果

一名 76 岁男性因持续牙龈出血到急诊就诊。血液样本分析出现了多个分析问题,最终导致多发性骨髓瘤的诊断。进一步的探索揭示了获得性因子 X 缺乏症,解释了持续的出血。没有同时存在淀粉样变性的证据。多发性骨髓瘤得到治疗,导致恶性肿瘤和出血倾向完全缓解。

结论

虽然在诊断为多发性骨髓瘤的患者中很少观察到凝血功能障碍,但当此类患者出现出血倾向时,考虑获得性因子 X 缺乏症变得相关。

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Acquired factor X deficiency in a multiple myeloma without amyloidosis: a case report.获得性因子 X 缺乏症合并多发性骨髓瘤而不伴淀粉样变性:一例报告。
Acta Clin Belg. 2023 Dec;78(6):524-528. doi: 10.1080/17843286.2023.2265650. Epub 2023 Oct 16.
2
[A patient with AL amyloidosis and severe factor X deficiency has been in complete haematological remission with normal factor X activity for 7 years following high-dose chemotherapy. A case study and literature review].[一名患有AL淀粉样变性和严重因子X缺乏症的患者在接受大剂量化疗后,血液学完全缓解,因子X活性正常,已持续7年。一项病例研究及文献综述]
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Acquired factor X deficiency in a patient with multiple myeloma: a rare case highlighting the significance of comprehensive evaluation and the need for antimyeloma therapy for bleeding diathesis.一名多发性骨髓瘤患者获得性因子X缺乏症:一个罕见病例凸显全面评估的重要性以及针对出血素质进行抗骨髓瘤治疗的必要性。
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引用本文的文献

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Acquired FX Deficiency in Multiple Myeloma without Concomitant Amyloidosis: A Rare Case Report.多发性骨髓瘤伴发非淀粉样变性的获得性因子X缺乏症:一例罕见病例报告
Acta Haematol. 2025 Mar 29:1-5. doi: 10.1159/000545479.
2
Navigating the Challenges of Factor X Deficiency: A Case Study.应对X因子缺乏症的挑战:一个案例研究
Cureus. 2024 Jul 22;16(7):e65084. doi: 10.7759/cureus.65084. eCollection 2024 Jul.
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Rediscovering hemostasis abnormalities in multiple myeloma: The new era.重新发现多发性骨髓瘤中的止血异常:新时代。
Heliyon. 2024 Jul 4;10(13):e34111. doi: 10.1016/j.heliyon.2024.e34111. eCollection 2024 Jul 15.