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首页> 外文期刊>International Journal of Research in Medical Sciences >A prospective study among cases of the pancytopenia on the basis of clinic-hematological analysis and bone marrow aspiration
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A prospective study among cases of the pancytopenia on the basis of clinic-hematological analysis and bone marrow aspiration

机译:基于临床血液学分析和骨髓穿刺术的全血细胞减少症病例前瞻性研究

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Background: Pancytopenia is consequence of many haematological condition with an extensive differential diagnosis. A prompt intervention is required to avoid complications. The severity and the underlying pathology determines the management and prognosis. Present study was conducted to assess the etiology, clinical profile and bone marrow morphology of pancytopenia. Methods: A prospective study was carried out among 50 consecutive patients with pancytopenia. Blood samples of the patients were analyzed for complete blood count and peripheral smear along with presence and absence of immature cells and abnormal cells. In bone marrow examination, morphology of all cells lineage, cellularity, parasite and abnormal cells were scrutinized. Trephine biopsy was done if indicated. Special investigations were done to confirm the diagnosis. Results: Among the 50 cases studied, age of the patients ranged from 1 to 70 years with a slight male predominance. Most common age group 11-20 years. Most of the patients presented with generalized weakness and fever. The commonest physical finding was pallor, followed by splenomegaly and hepatomegaly. The commonest marrow finding was hyper cellularity with megaloblastic erythropoiesis. The commonest cause for pancytopenia was megaloblastic anemia. Conclusions: The present study concludes that hematological investigations along with other supportive tests are helpful to diagnose or to rule out the causes of pancytopenia. Megaloblastic anemia is commonest cause of pancytopenia in most Indian and subcontinent studies. Substantial number of patients had reversible etiology. Hence complete work up including clinical details with hematological examination along with bone marrow study will lead to early and proper diagnosis and management.
机译:背景:全血细胞减少症是许多血液学疾病的结果,具有广泛的鉴别诊断。需要及时干预以避免并发症。严重程度和潜在病理决定了治疗和预后。进行本研究以评估全血细胞减少症的病因,临床概况和骨髓形态。方法:对50例全血细胞减少症患者进行了前瞻性研究。分析患者的血样的全血细胞计数和外周涂片以及是否存在未成熟细胞和异常细胞。在骨髓检查中,检查所有细胞谱系,细胞结构,寄生虫和异常细胞的形态。如果有指征,则进行冰毒活检。进行了专门调查以确认诊断。结果:在研究的50例病例中,患者年龄为1至70岁,男性占优势。最常见的年龄组是11-20岁。大多数患者表现为全身无力和发烧。最常见的体格检查是苍白,其次是脾肿大和肝肿大。最常见的骨髓发现是具有巨幼红细胞生成的高细胞性。引起全血细胞减少的最常见原因是巨幼细胞性贫血。结论:本研究得出的结论是,血液学检查以及其他支持性检查有助于诊断或排除全血细胞减少症的原因。在大多数印度和次大陆研究中,巨幼细胞性贫血是引起全血细胞减少的最常见原因。大量病因可逆。因此,包括血液学检查的临床细节以及骨髓研究在内的完整检查将导致早期和适当的诊断和治疗。

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