Complete clinicopathological profile and etiological spectrum of pancytopenia in adult patients attending a tertiary care referral center in Eastern India

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Srishtidhar Mangal, S. Sinha
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Abstract

Introduction: Pancytopenia is a common hematological condition manifesting as a simultaneous decrease in formed elements of blood-red blood cell, white blood cell, and platelets. It happens in many illnesses, ranging from simple drug-induced bone marrow hypoplasia, megaloblastic anemia to fatal bone marrow aplasias and leukemias. Identifying the correct etiology and clinicopathological spectrum of pancytopenia helps in implementing timely and appropriate treatment. Hence, this study was undertaken for profiling pancytopenia and we chose to focus on adult patient only. Materials and Methods: The present study was an observational, cross-sectional study conducted at a tertiary care referral center in Kolkata which included 91 cases of pancytopenia over a period of 2 years. Cases were of both sexes and age >20 years who were not on any kind of drug therapy. Cases were evaluated clinically and with complete set of relevant pathological parameters. Results: In our study, the most common etiology was aplastic anemia (24.2%), followed by myelodysplastic syndrome (17.6%) and acute leukemia (14.3%). The most common age range being 21–30 years and most common symptom being progressive pallor. Anisocytosis, reticulocytosis, hypercellular marrow, and no marrow fibrosis were the most common hematological pictures. Severe pancytopenia was seen in aplastic anemia and acute leukemia. Conclusion: The present study concludes that detailed clinical history and complete hematological investigations including bone marrow studies in patients presenting with symptoms of pancytopenia are essential in understanding the disease process and to delineate the causes of pancytopenia. We found aplastic anemia to be the most common etiology in our study, consistent with the studies of Kumar et al. and Niazi et al. The following core competencies are addressed in this article: Practice-based learning and improvement, Patient care and procedural skills, Medical knowledge, and Professionalism
完整的临床病理资料和全血细胞减少症的病因谱在成年患者参加三级保健转诊中心在印度东部
简介:全血细胞减少症是一种常见的血液病,表现为血液中红细胞、白细胞和血小板的形成元素同时减少。它发生在许多疾病中,从简单的药物诱导的骨髓发育不全、巨幼细胞性贫血到致命的骨髓发育不良和白血病。确定全血细胞减少症的正确病因和临床病理谱有助于实施及时和适当的治疗。因此,本研究旨在分析全血细胞减少症,我们选择仅关注成年患者。材料和方法:本研究是一项在加尔各答三级护理转诊中心进行的观察性横断面研究,包括2年内91例全血细胞减少症。病例为未接受任何药物治疗的性别和年龄>20岁的患者。对病例进行了临床评估,并提供了一套完整的相关病理参数。结果:在我们的研究中,最常见的病因是再生障碍性贫血(24.2%),其次是骨髓增生异常综合征(17.6%)和急性白血病(14.3%)。最常见的年龄范围为21-30岁,最常见症状为进行性苍白。无细胞增生症、网织细胞增多症、骨髓细胞增多症和无骨髓纤维化是最常见的血液学图片。再生障碍性贫血和急性白血病患者出现严重的全血细胞减少症。结论:本研究得出结论,对出现全血细胞减少症症状的患者进行详细的临床病史和完整的血液学研究,包括骨髓研究,对于了解疾病过程和描述全血细胞减少的原因至关重要。我们发现再生障碍性贫血是我们研究中最常见的病因,这与Kumar等人和Niazi等人的研究一致。本文讨论了以下核心能力:基于实践的学习和改进、患者护理和程序技能、医学知识和专业精神
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
International Journal of Academic Medicine
International Journal of Academic Medicine Social Sciences-Education
CiteScore
1.10
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0.00%
发文量
8
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