The Benign Clone Causing Aplastic Anaemia

IF 0.6 Q4 HEMATOLOGY
S. McCann, A. Piccin
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引用次数: 0

Abstract

Severe Aplastic Anaemia (SAA) is a rare benign disease but carries a high-mortality rate unless treated in a specialised centre. Overwhelming laboratory and clinical evidence points to an autoimmune pathogenesis; although, the aetiology remains obscure in the majority of cases. The differential diagnosis in older patients is problematical and a diagnosis of hypoplastic myelodysplasia remains difficult. This review points out the difficulty in diagnosis without a specific test. Future research needs to define a specific diagnostic test and refine therapeutic interventions.
良性克隆导致再生障碍性贫血
严重再生障碍性贫血(SAA)是一种罕见的良性疾病,但除非在专门的中心治疗,否则死亡率很高。大量的实验室和临床证据指向自身免疫发病机制;虽然,在大多数情况下,病因尚不清楚。老年患者的鉴别诊断是有问题的,骨髓发育不良的诊断仍然很困难。这篇综述指出了在没有具体的检查的情况下诊断的困难。未来的研究需要确定一个具体的诊断测试和完善治疗干预。
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
Thalassemia Reports
Thalassemia Reports HEMATOLOGY-
自引率
0.00%
发文量
17
审稿时长
10 weeks
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