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全血细胞减少症:一项临床血液学研究。

Pancytopenia: a clinico hematological study.

作者信息

Gayathri B N, Rao Kadam Satyanarayan

机构信息

Department of Pathology, SDUMC, Tamaka, Kolar, India.

出版信息

J Lab Physicians. 2011 Jan;3(1):15-20. doi: 10.4103/0974-2727.78555.

DOI:10.4103/0974-2727.78555
PMID:21701657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3118050/
Abstract

BACKGROUND

Pancytopenia is a relatively common hematological entity. It is a striking feature of many serious and life-threatening illnesses, ranging from simple drug-induced bone marrow hypoplasia, megaloblastic anemia to fatal bone marrow aplasias and leukemias. The severity of pancytopenia and the underlying pathology determine the management and prognosis. Thus, identification of the correct cause will help in implementing appropriate therapy.

OBJECTIVES

To study the clinical presentations in pancytopenia due to various causes; and to evaluate hematological parameters, including bone marrow aspiration.

MATERIALS AND METHODS

It was a prospective study, and 104 pancytopenic patients were evaluated clinically, along with hematological parameters and bone marrow aspiration in Hematology Unit, Department of Pathology, JJMMC, Davanagere, during the period of September 2005 to September 2007.

RESULTS

Among 104 cases studied, age of patients ranged from 2 to 80 years with a mean age of 41 years, and male predominance. Most of the patients presented with generalized weakness and fever. The commonest physical finding was pallor, followed by splenomegaly and hepatomegaly. Dimorphic anemia was the predominant blood picture. Bone marrow aspiration was conclusive in all cases. The commonest marrow finding was hypercellularity with megaloblastic erythropoiesis. The commonest cause for pancytopenia was megaloblastic anemia (74.04%), followed by aplastic anemia (18.26%).

CONCLUSION

Thepresent study concludes that detailed primary hematological investigations along with bone marrow aspiration in cytopenic patients are helpful for understanding disease process and to diagnose or to rule out the causes of cytopenia. These are also helpful in planning further investigations and management.

摘要

背景

全血细胞减少是一种相对常见的血液学病症。它是许多严重且危及生命疾病的显著特征,范围从简单的药物性骨髓发育不全、巨幼细胞贫血到致命的骨髓再生障碍和白血病。全血细胞减少的严重程度及潜在病理机制决定了治疗方法和预后。因此,确定正确病因有助于实施恰当的治疗。

目的

研究各种病因导致的全血细胞减少的临床表现;并评估血液学参数,包括骨髓穿刺检查。

材料与方法

这是一项前瞻性研究,于2005年9月至2007年9月期间,在达瓦纳盖里JJMMC病理学系血液科,对104例全血细胞减少患者进行了临床评估、血液学参数检测及骨髓穿刺检查。

结果

在研究的104例病例中,患者年龄从2岁至80岁不等,平均年龄41岁,男性居多。大多数患者表现为全身无力和发热。最常见的体征是面色苍白,其次是脾肿大和肝肿大。双形性贫血是主要的血象表现。所有病例的骨髓穿刺检查都有诊断意义。最常见的骨髓表现是细胞增多伴巨幼红细胞生成。全血细胞减少最常见的病因是巨幼细胞贫血(74.04%),其次是再生障碍性贫血(18.26%)。

结论

本研究得出结论,对血细胞减少患者进行详细的原发性血液学检查及骨髓穿刺,有助于了解疾病过程,诊断或排除血细胞减少的病因。这些检查也有助于规划进一步的检查和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/ebb6a1ac8629/JLP-3-15-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/3c9b428b6d65/JLP-3-15-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/5162fb2c457f/JLP-3-15-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/44d9805dd83a/JLP-3-15-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/4b18f6b6deed/JLP-3-15-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/bc32b96ef4c7/JLP-3-15-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/ebb6a1ac8629/JLP-3-15-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/3c9b428b6d65/JLP-3-15-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/5162fb2c457f/JLP-3-15-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/44d9805dd83a/JLP-3-15-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/4b18f6b6deed/JLP-3-15-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/bc32b96ef4c7/JLP-3-15-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0df7/3118050/ebb6a1ac8629/JLP-3-15-g009.jpg

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