Indian Journal of Pathology and Microbiology (Jan 2022)

Cold autoimmune hemolytic anemia with myelodysplastic syndrome: Not just an “Open and Shut case”

  • Deepti Mutreja,
  • Gourang Paliwal,
  • Vishal Mangal,
  • Amit K Biswas

DOI
https://doi.org/10.4103/IJPM.IJPM_981_20
Journal volume & issue
Vol. 65, no. 1
pp. 195 – 197

Abstract

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Myelodysplastic syndromes (MDSs) are clonal hematopoietic stem cell neoplasms characterized by bone marrow failure leading to ineffective hematopoiesis, dyspoiesis, and cytopenias with a risk of progression to acute leukemia. Immunological syndromes have been reported to occur along with MDS in literature. However, cold autoimmune hemolytic anemia (AIHA) has rarely been reported in association with MDS. Herein, we report a case of an elderly male who presented with fever and cytopenias. He was being treated as a case of megaloblastic anemia in the past with no response to therapy. At present admission, the peripheral blood smear examination revealed red cell agglutination, thrombocytopenia with 4% blasts. Cold agglutinin disease was confirmed by a thermal agglutination test and bone marrow evaluation showed adequate megakaryocytes with 10% blasts; consistent with the diagnosis of MDS with excess blasts (MDS-EB2). Cytogenetic studies revealed multiple abnormalities. This report is being discussed in view of its rarity of presentation of cold AIHA with MDS.

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