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在一家三级护理中心进行的全血细胞减少症的临床特征和病因谱的横断面研究。

A cross-sectional study of the clinical profile and aetiological spectrum of pancytopenia in a tertiary care centre.

机构信息

Department of Medicine, Medical College and Hospital Kolkata, 88 College Street, Kolkata 700073, India.

出版信息

Singapore Med J. 2010 Oct;51(10):806-12.

Abstract

INTRODUCTION

Pancytopenia is a common haematological problem. It is suspected when a patient presents with anaemia, prolonged fever and a bleeding tendency. Pancytopenia has multiple causes, but the frequency of these causes has been reported in a limited number of studies. The present study was conducted to assess the aetiological pattern, clinical profile and bone marrow morphology of pancytopenia patients.

METHODS

A total of 111 adult pancytopenia patients aged 13 to 65 years were studied during a one-year period to determine their clinical features, peripheral blood pictures and bone marrow morphologies. The aetiological pattern was assessed through the relevant investigations in the respective patients.

RESULTS

45.95 percent of the pancytopenic patients had a hypocellular marrow, while 54.05 percent had normocellular or hypercellular marrow. Idiopathic aplastic anaemia (20.72 percent) was the commonest cause of pancytopenia, followed by hypersplenism due to chronic liver disease (11.71 percent). Other important causes were kala-azar (nine percent), megaloblastic anaemia, systemic lupus erythematosus (SLE), infections and drug inducement. Infections such as kala-azar, falciparum malaria and enteric fever, megaloblastic anaemia as well as SLE were found to be treatable and reversible causes of pancytopenia.

CONCLUSION

As a large number of pancytopenic patients have a reversible aetiology, early and proper diagnosis may be life-saving.

摘要

简介

全血细胞减少是一种常见的血液学问题。当患者出现贫血、长期发热和出血倾向时,就会怀疑全血细胞减少症。全血细胞减少症有多种原因,但这些原因的频率在有限的研究中有所报道。本研究旨在评估全血细胞减少症患者的病因模式、临床特征和骨髓形态学。

方法

在一年的时间里,共研究了 111 名年龄在 13 至 65 岁之间的成人全血细胞减少症患者,以确定他们的临床特征、外周血象和骨髓形态。通过对各患者的相关检查来评估病因模式。

结果

45.95%的全血细胞减少症患者骨髓细胞减少,而 54.05%的患者骨髓细胞正常或增多。特发性再生障碍性贫血(20.72%)是全血细胞减少症最常见的病因,其次是慢性肝病引起的脾功能亢进(11.71%)。其他重要的病因包括黑热病(9%)、巨幼细胞性贫血、系统性红斑狼疮(SLE)、感染和药物诱导。感染(如黑热病、恶性疟原虫疟疾和伤寒)、巨幼细胞性贫血以及 SLE 被发现是可治疗和可逆的全血细胞减少症病因。

结论

由于大量全血细胞减少症患者的病因是可逆的,因此早期和适当的诊断可能是救命的。

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