Case Report: Severe mixed autoimmune hemolytic anemia associated with acute cytomegalovirus infection in an immunocompetent adult - Report - MDSpire
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Case Study: Acute Cytomegalovirus Infection Leading to Severe Mixed Autoimmune Hemolytic Anemia in an Immunocompetent Individual

  • By

  • Junjie Hou

  • Yanhong Ding

  • Huiyao Chen

  • Min Liao

  • Chun Feng

  • Jihao Zhou

  • Guoqiang Li

  • Peng Ke

  • Feichang Du

  • September 15, 2026

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Clinical Report: Acute Cytomegalovirus Infection Leading to Severe Mixed Autoimmune Hemolytic Anemia

Overview

This case study presents a 59-year-old immunocompetent man who developed severe mixed autoimmune hemolytic anemia (AIHA) associated with acute cytomegalovirus (CMV) infection. Comprehensive immunohematologic assessment confirmed the diagnosis, revealing both warm and cold autoantibodies, and combination therapy, including antiviral and immunomodulatory treatments, effectively managed the condition.

Background

Cytomegalovirus (CMV) infection can lead to various clinical manifestations, including autoimmune hemolytic anemia (AIHA), which is rare in immunocompetent individuals. Mixed AIHA, characterized by the presence of both warm and cold autoantibodies, complicates diagnosis and management. Understanding the serologic patterns and treatment approaches is crucial for effective patient care, particularly given the infrequency of this condition in immunocompetent hosts.

Data Highlights

The patient presented with severe hemolytic anemia, with a hemoglobin level of 40 g/L and significant laboratory evidence of acute hemolysis, including erythrocyte-bound IgG, IgA, IgM, and C3d. An IgM cold agglutinin was detected at a titer of 1:128, indicating the presence of both warm and cold autoantibodies.

Key Findings

  • Severe mixed AIHA can occur in immunocompetent adults following CMV infection.
  • Diagnosis of mixed AIHA requires comprehensive immunohematologic testing beyond routine direct antiglobulin test (DAT).
  • Both warm-reactive IgG and cold-reactive IgM autoantibodies were identified in the patient.
  • Combination therapy, including antiviral and immunomodulatory treatments, effectively managed the patient's hemolysis.
  • Accurate subtyping of AIHA is essential for appropriate treatment and management.

Clinical Implications

Comprehensive immunohematologic testing is necessary for accurate diagnosis and effective management of mixed AIHA in patients with severe hemolytic anemia and recent CMV infection.

Conclusion

This case highlights the recognition of mixed AIHA in the context of CMV infection and the importance of thorough diagnostic evaluation and targeted treatment strategies.

Related Resources & Content

  1. Frontiers in Immunology, Case Report: Genetically primed hyperinflammation: cytomegalovirus-triggered HLH-like syndrome in an adolescent with a gain-of-function STING1 (p.Arg281Trp) variant with novel autosomal dominant inheritance and atypical presentation
  2. Open Forum Infectious Diseases, Understanding Positive Cytomegalovirus IgM Test Outcomes in Hospitalized Immunocompetent Adults With Suspected Acute Infection: A Multicenter Analysis
  3. American Journal of Hematology, Late Cytomegalovirus Infections After Allogeneic Hematopoietic Cell Transplant
  4. jadpro, Role of Preemptive Cytomegalovirus Hyperimmunoglobulin in Cytomegalovirus Viremia Following Stem Cell Transplant: An Integrative Review
  5. Autoimmune Hemolytic Anemias: Challenges in Diagnosis and Therapy
  6. Autoimmune Hemolytic Anemias: Challenges in Diagnosis and Therapy
  7. Sustained improvements in patient-reported outcomes after long-term sutimlimab in patients with cold agglutinin disease: results from the CADENZA study open-label extension - PMC
  8. Infection Control in Healthcare Personnel: Epidemiology and Control of Selected Infections Transmitted Among Healthcare Personnel and Patients

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