Evaluation of Reticulin Fibrosis in Benign Hematologic Disorders in Lahore, Pakistan: A Cross-Sectional Study

Objective: To assess reticulin fibrosis in benign hematologic disorders and to understand the impact of benignhematologic disorders on the immune system.Study Design: Cross-sectional study.Place and Duration of Study: The study was conducted at the Department of Hematology, Sheikh ZayedHospital, Lahore, Pakistan from January 2023 to June 2023.Methods: Patients who had benign hematologic disorders, such as iron deficiency anemia, MegaloblasticAnemia, Aplastic Anemia, and Immune Thrombocytopenic Purpura, were included in the research. Patientswith Malignant hematologic disorders and Individuals undergoing chemotherapy for any malignant diseasewere excluded. There were 96 cases total in the sample, 24 for each illness. Following processing in the histology department, the data for reticulin fibers were analyzed using bone marrow samples from the anterioriliac spine. An institutional ethics panel approved the research, and informed consent was acquired.Results: The study found that the gender distribution of cases was significantly different among the fourgroups. The average age of cases was not different among the four groups. Still, the Immune Thrombocytopenic Purpura group had the lowest average age of 40.5 years, and the Aplastic anemia group had the highest average age of 46.7 years. Among the hematological parameters, the hemoglobin level was the highest among the Immune Thrombocytopenic Purpura group, with an average of 10.8±1.9 g/dl. The median total leukocyte count for Iron Deficiency Anemia was 6.3, while the median total leukocyte count for megaloblastic anemia was 3.2, Aplastic Anemia was 1.8, and Immune Thrombocytopenic Purpura was 8.0. The median RDW count for Iron Deficiency Anemia was 42.0, Megaloblastic Anemia was 50.0, Aplastic Anemia was 48.5, and ITP was 48.0.Conclusion: The study concluded that female gender, higher Hemoglobin level, higher MCH, Red blood cellcount, and lower platelet count may also help support the diagnosis of Immune Thrombocytopenic Purpura.Identifying these parameters as diagnostic markers requires further research to confirm their status. How to cite this: Shabbir Y, Farooq N, Akhter F, Virk AA, Fayyaz M, Eyyaz M. Evaluation of Reticulin Fibrosis in Benign Hematologic Disorders in Lahore, Pakistan: A Cross-Sectional Study. Life and Science. 2025; 6(2): 156-162. doi: http://doi.org/10.37185/LnS.1.1.578