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慢性淋巴细胞白血病中的自身免疫性血细胞减少症

Autoimmune cytopenias in chronic lymphocytic leukemia.

作者信息

Haider M Shabih, Khan Saleem Ahmed, Shahid Samra

机构信息

Dr. Mohammad Shabih Haider, MBBS, Department of Pathology (Haematology Section), Army Medical College, Rawalpindi, Pakistan.

Dr. Saleem Ahmed Khan, FCPS, Department of Pathology (Haematology Section), Army Medical College, Rawalpindi, Pakistan.

出版信息

Pak J Med Sci. 2019 Sep-Oct;35(5):1334-1338. doi: 10.12669/pjms.35.5.369.

Abstract

OBJECTIVE

To determine the frequency of autoimmune cytopenias in chronic lymphocytic leukemia.

METHODS

This cross sectional study was carried out at Department of Hematology, Army Medical College Rawalpindi, in collaboration with Military Hospital Rawalpindi and Armed Forces institute of Pathology Rawalpindi from 1st January 2018 to 1st October 2018. Sample size of 64 was calculated using WHO calculator. Age and gender of patients was noted. Frequency of autoimmune hemolytic anaemia, immune thrombocytopenic purpura, pure red cell aplasia and autoimmune agranulocytosis were determined in diagnosed patients of chronic lymphocytic leukemia by various laboratory tests in our study population.

RESULTS

A total of 64 patients were included in the study, 53 (82.8%) were males and 11(17.2%) were females. Mean age of patients was 65 years. Autoimmune hemolytic anaemia was observed in 5/64 (7.8%) of patients. Immune thrombocytopenic purpura was seen in 2/64 (3.1%) patients. Autoimmune granuloytopenia and pure red cell aplasia were not seen in any patient.

CONCLUSION

Autoimmune hemolytic anaemia and immune thrombocytopenic purpura are the most common causes of immune cytopenias in patients of CLL. Immune cytopenias should always be identified by laboratory tests as their management differs from other cytopenias which occur due to various other causes.

摘要

目的

确定慢性淋巴细胞白血病中自身免疫性血细胞减少症的发生率。

方法

本横断面研究于2018年1月1日至2018年10月1日在拉瓦尔品第陆军医学院血液科进行,与拉瓦尔品第军事医院和拉瓦尔品第武装部队病理研究所合作。使用世界卫生组织计算器计算出样本量为64。记录患者的年龄和性别。通过我们研究人群中的各种实验室检查,确定慢性淋巴细胞白血病确诊患者中自身免疫性溶血性贫血、免疫性血小板减少性紫癜、纯红细胞再生障碍和自身免疫性粒细胞缺乏症的发生率。

结果

本研究共纳入64例患者,其中男性53例(82.8%),女性11例(17.2%)。患者的平均年龄为65岁。5/64(7.8%)的患者观察到自身免疫性溶血性贫血。2/64(3.1%)的患者出现免疫性血小板减少性紫癜。未在任何患者中发现自身免疫性粒细胞减少和纯红细胞再生障碍。

结论

自身免疫性溶血性贫血和免疫性血小板减少性紫癜是慢性淋巴细胞白血病患者免疫性血细胞减少症的最常见原因。免疫性血细胞减少症应始终通过实验室检查来识别,因为其治疗方法与因其他各种原因引起的其他血细胞减少症不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c9a/6717446/b42348e09cfc/PJMS-35-1334-g001.jpg

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