Etiological spectrum of pancytopenia in adults based on hematological parameters and bone marrow studies.

IF 2.3 4区 医学 Q2 HEMATOLOGY Expert Review of Hematology Pub Date : 2024-11-01 Epub Date: 2024-10-29 DOI:10.1080/17474086.2024.2421374
Umera Saleem, Hamza Tariq, Shahroz Alam, Ahmed Faraz Zafar, Urwah Tanveer, Muhammad Hamza Khan
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Abstract

Background: This study aimed to investigate the demographic, clinical, and diagnostic aspects of adult pancytopenia while exploring its etiological spectrum through hematological parameters and bone marrow studies.

Research design and methods: This observational study involved 117 adult individuals ranging from 13 to 85 years who presented with pancytopenia. A comprehensive examination of demographic features, hematological parameters, clinical presentations, and physical findings, including liver and spleen characteristics, was conducted. Additionally, serological analyses for HBsAg and Anti HCV were performed. The diagnostic spectrum was determined through bone marrow studies.

Results: Pancytopenia manifested with varied clinical symptoms, with generalized weakness (72.65%), fever (64.1%), dyspnea (54.70%), bleeding (34.2%), and weight loss (25.6%) being prominent. Physical examination revealed a range of liver and spleen characteristics, with hepatomegaly observed in 32.48% and splenomegaly in 44.4% of cases. Serological findings indicated HBsAg positivity in 8.5% and Anti HCV positivity in 21.37% of cases. The diagnostic distribution encompassed diverse conditions, with aplastic anemia (17.1%), megaloblastic anemia (12.8%), and myelodysplastic syndromes (12.8%) being prevalent.

Conclusions: This study provides a comprehensive overview of the demographic, clinical, and diagnostic aspects of pancytopenia. The observed prevalence of different diagnoses underscores the necessity of a thorough evaluation, including bone marrow studies, for accurate diagnosis and appropriate management.

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基于血液学参数和骨髓研究的成人全血细胞减少症病因谱。
研究背景本研究旨在调查成人全血细胞减少症的人口统计学、临床和诊断方面的情况,同时通过血液学参数和骨髓研究探索其病因谱:这项观察性研究涉及 117 名患有全血细胞减少症的成人,年龄从 13 岁到 85 岁不等。研究人员对这些患者的人口统计学特征、血液学参数、临床表现和体格检查结果(包括肝脏和脾脏特征)进行了全面检查。此外,还进行了 HBsAg 和抗 HCV 血清学分析。通过骨髓研究确定了诊断谱:全血细胞减少症表现出多种临床症状,其中以全身乏力(72.65%)、发热(64.1%)、呼吸困难(54.70%)、出血(34.2%)和体重减轻(25.6%)最为突出。体格检查显示一系列肝脏和脾脏特征,32.48%的病例观察到肝脏肿大,44.4%的病例观察到脾脏肿大。血清学检查结果显示,8.5%的病例呈 HBsAg 阳性,21.37%的病例呈抗 HCV 阳性。诊断分布包括多种疾病,其中再生障碍性贫血(17.1%)、巨幼细胞性贫血(12.8%)和骨髓增生异常综合征(12.8%)最为常见:本研究全面概述了全血细胞减少症的人口统计学、临床和诊断方面的情况。所观察到的不同诊断的发病率强调了全面评估(包括骨髓研究)对准确诊断和适当治疗的必要性。
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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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