Asian Journal of Biological and Life Sciences logo
Article

Myelodysplastic Syndrome: Raeb-1 in A 58-Year-Old Male: A Case Report from Andhra Pradesh, India

1, 1, 1, 1, 1, 1, 1, 1, 2

  1. 1Department of Pharmacy Practice, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh, INDIA.
  2. 2Department of Pharmaceutics, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh, INDIA.

CORRESPONDENCE

Pavan Kumar Yanamadala

Department of Pharmacy Practice, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh, INDIA.

pavan.yanamadala@gmail.com

Received: 11-02-2026; Revised: 06-03-2026; Accepted: 28-04-2026.

Volume 15, Issue 1 · pp. 235-239 · 2026 · DOI: 10.5530/ajbls.20260052

ABSTRACT

Myelodysplastic Syndromes (MDS) represent clonal hematopoietic disorders that are marked by ineffective hematopoiesis, peripheral cytopenias, and a fluctuating risk of progression to acute myeloid leukaemia. Research conducted in India has revealed an earlier age of onset and a greater prevalence of adverse cytogenetic profiles in comparison to Western populations; however, comprehensive case-based documentation is still lacking. We report a case of a 58-year-old male farmer from Guntur District, Andhra Pradesh, who experienced progressive dyspnea, fatigue, recurrent low-grade fever, gum bleeding, and spontaneous bruising. Examination revealed pallor, petechiae, and mild splenomegaly. Laboratory tests showed pancytopenia with macrocytic anaemia, hypogranular neutrophils, and giant platelets. Bone marrow aspiration indicated hypercellularity with multilineage dysplasia, ring sideroblasts, and 6% myeloblasts. Cytogenetic analysis revealed an isolated deletion of chromosome 5q. Based on these findings, a diagnosis of MDS - Refractory Anaemia with Excess Blasts-1 (RAEB-1) was made. The patient was treated with supportive transfusions, empirical antibiotics for febrile neutropenia, and subcutaneous azacitidine. This case exemplifies the diversity of MDS, consistent with Indian research that indicates an earlier onset and differing prognostic characteristics. It underscores the importance of documenting individual cases to connect epidemiological disparities between Western and Indian populations. This case underscores the clinical and cytogenetic characteristics of MDS in an Indian patient, drawing attention to the diagnostic difficulties and treatment considerations in settings with limited resources. Comprehensive regional case reports are crucial for enhancing the understanding of disease biology and outcomes within Indian populations.

KEYWORDS

Open in new tab

REFERENCES

As published

Showing references and in-text citations exactly as published.

    Cite this article

    SELECT FORMAT

    Tamanam, R. S., Puli, C., Thinnavalli, T. S., Gannamaneni, A. C., Konkimalla, S. K., Taviti, R. K., Devarapalli, R. H., Yanamadala, P. K., & Nadendla, R. R. (2026). Myelodysplastic Syndrome: Raeb-1 in A 58-Year-Old Male: A Case Report from Andhra Pradesh, India. Asian Journal of Biological and Life Sciences, 15(1), 235-239. https://doi.org/10.5530/ajbls.20260052

    Copyright and licence

    © 2026 Author(s)

    This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. CC BY 4.0