[Acquired FX deficiency: a case report and literature review].

Q3 Medicine
J Zhang, W Liu, Y H Wang, R C Yang, L Zhang, F Xue
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引用次数: 0

Abstract

Objective: To introduce the clinical features, laboratory findings, diagnostic approaches, and treatment of acquired factor X deficiency. Methods: This study reviewed a case of primary light-chain amyloidosis with acquired factor X deficiency admitted to our hospital. The patient's clinical course and diagnostic process were described, and a literature review was conducted. Results: The patient, a 69-year-old male, was admitted to our hospital due to abdominal bleeding. He was diagnosed with primary light-chain amyloidosis complicated by acquired factor X deficiency. Recurrent bleeding was attributed to amyloid deposits in peripheral blood vessels and organs, which adsorbed circulating factor X, causing its sequestration in the reticuloendothelial system (e.g. the spleen) and leading to decreased factor X levels. After active hemostasis and treatment of the underlying disease, the patient was discharged. Conclusion: This case provides insights and a reference for the diagnosis and management of the rare clinical presentation of acquired coagulation factor deficiency.

【获得性FX缺乏症1例报告及文献复习】。
目的:介绍获得性因子X缺乏症的临床特点、实验室表现、诊断方法及治疗方法。方法:回顾我院收治的一例原发性轻链淀粉样变性合并获得性因子X缺乏症。描述患者的临床病程和诊断过程,并进行文献复习。结果:患者男,69岁,因腹部出血入院。他被诊断为原发性轻链淀粉样变性合并获得性因子X缺乏。反复出血的原因是周围血管和器官中的淀粉样蛋白沉积吸附了循环因子X,使其在网状内皮系统(如脾脏)中被隔离,导致因子X水平下降。经积极止血和治疗基础疾病后,患者出院。结论:本病例对获得性凝血因子缺乏这一罕见临床表现的诊断和治疗有一定的参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
100
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