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Autoimmune Hemolytic Anemia as an Initial Manifestation of Splenic Marginal Zone Lymphoma
Neeti Nachammai K M1, Vengadakrishnan K1, Suja Lakshmanan2,1
1General Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Abstract:
Autoimmune hemolytic anemia (AIHA) is caused by autoantibodies that target and destroy the individual's own red blood cells (RBCs). Warm AIHA is due to antibodies that are active at body temperature and are the most common type of AIHA. Herein, we report a 49-year-old woman who presented with breathlessness, easy fatiguability, and palpitations with blood picture showing severe anemia requiring multiple blood transfusions, leucocytosis, Direct Coombs Test (DCT) positivity, and elevated lactate dehydrogenase (LDH). The patient later developed increasing leukocytosis, for which bone marrow biopsy and immunophenotyping using flow cytometry were done, confirming the presence of underlying splenic marginal zone lymphoma resulting in secondary AIHA. The patient was referred to the hematology department and was started on treatment with steroids and rituximab.
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