Print ISSN:-2249-8176

Online ISSN:-2348-7682

CODEN : PJMSD7

Current Issue

Year 2024

Volume: 14 , Issue: 2

Indexed by

Indexed by DOAJ

Article Access statistics

Viewed: 140

Emailed: 0

PDF Downloaded: 460

Panacea Journal of Medical Sciences


Clinical and haematological evaluation of Pancytopenia : A cross sectional study in a tertiary care centre of Western Odisha


Full Text PDF Share on Facebook Share on Twitter


Original Article

Author Details : Binod Kumar Sahu, Pushpanjali Mishra, Kshetra Mohan Tudu, Sunanda Nayak*

Volume : 13, Issue : 3, Year : 2023

Article Page : 612-618

https://10.18231/j.pjms.2023.113

Article Metrics



Suggest article by email


Abstract

Background: Pancytopenia is the outcome of bone marrow abnormalities and progresses with thrombocytopenia, leukopenia, and anemia. The frequently reported clinical manifestations of pancytopenia include infections, hemorrhage, dyspnea, and pallor. This study aimed to improve the diagnostic assessment of pancytopenia by underlying its potential haematological and clinical parameters. 
Materials and Methods: The enrolled patients underwent haematological and clinical assessments for pancytopenia at Veer Surendra Sai Institute of Medical Science and Research, Odisha, India. The pancytopenia assessment parameters included peripheral blood smear, reticulocyte count, mean corpuscular hemoglobin concentration, mean corpuscular hemoglobin, mean corpuscular volume, differential count, total platelet count, total leukocyte count, red blood cell count, and hemoglobin level. Patients also underwent bone marrow aspiration and biopsy for diagnostic investigation.
Results: The bone marrow study and peripheral smears were conducted on eighty-eight patients, and findings revealed the incidence of potential pancytopenia causes including, malaria (1%, n=1), multiple myeloma (1%, n=1), metastatic adenocarcinoma (1%, n=1), hemophagocytic lymphohistiocytosis (1%, n=1), tubercular granuloma (1%, n=1), sickle cell crisis (2%, n=2), hypersplenism (3%, n=3), myelodysplastic syndromes (3%, n=3), acute lymphoblastic leukemia (3%, n=3), acute myeloid leukemia (7%, n=6), aplastic anemia (32%, n=28) and megaloblastic anemia (43% n=38). 
Conclusion: Pancytopenia is predominantly caused by megaloblastic anemia and aplastic anemia, respectively. The frequently reported clinical manifestations include bleeding, fever, and weakness. The diagnostic affirmations rely on bone marrow biopsy/aspiration.
 
Keywords: Pancytopenia, Bone marrow biopsy, Aspiration, Aplastic anemia, Megaloblastic anemia


How to cite : Sahu B K, Mishra P, Tudu K M, Nayak S, Clinical and haematological evaluation of Pancytopenia : A cross sectional study in a tertiary care centre of Western Odisha. Panacea J Med Sci 2023;13(3):612-618

Copyright © 2023 by author(s) and Panacea J Med Sci. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License (creativecommons.org)