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Updated: Aug 26, 2025

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
Published on: October 3, 2018
Myelodysplastic Syndrome in a Patient With Common Variable Immunodeficiency: A Rare Occurrence
Nihas R Mateti1, Raju K Vaddepally2, Priya Elsa Skaria3
1Department of Medicine, Osmania Medical College, Hyderabad, IND.
Insights
Common variable immunodeficiency (CVID) rarely associates with myelodysplastic syndrome (MDS). This case highlights a young patient with CVID who developed MDS with excess blasts-2, requiring azacitidine treatment.
Area of Science:
- Hematology
- Immunology
Background:
- Common variable immunodeficiency (CVID) is a primary immunodeficiency characterized by impaired B-cell function and antibody production.
- CVID commonly presents with sinopulmonary and gastrointestinal issues and has a known association with acute myeloid leukemia.
- The association between CVID and myelodysplastic syndrome (MDS) is exceptionally rare.
Observation:
- A 26-year-old patient with CVID presented with severe thrombocytopenia.
- Bone marrow biopsy showed hypercellular marrow with increased CD34 blasts and loss of the Y chromosome.
- The patient was diagnosed with MDS with excess blasts-2, classified as intermediate-risk.
Findings:
- The patient received azacitidine, a hypomethylating agent, for MDS treatment.
- Referral for allogeneic stem cell transplant was made for further management.
- This case underscores a rare complication of CVID.
Implications:
- This case expands the known spectrum of CVID complications.
- Highlights the importance of considering hematologic malignancies in CVID patients.
- Suggests potential need for closer hematologic monitoring in CVID patients.
Abstract:
Common variable immunodeficiency (CVID) is a primary immunodeficiency disorder caused by impaired B-cell function and antibody production. It commonly presents with chronic sinopulmonary and gastrointestinal manifestations. It is also associated with transformation to acute myeloid leukemia. However, the association of CVID with myelodysplastic syndrome (MDS) is rare. This case report aims to present one such rare association in a 26-year-old patient presenting with severe thrombocytopenia. Bone marrow biopsy revealed hypercellular marrow with 80-90% cellularity along with an increase in CD34 blasts. Cytogenetics revealed loss of the Y chromosome. Diagnosis of MDS with excess blasts-2 was confirmed with a Revised International Prognostic Scoring System score of 4, placing the patient in the intermediate-risk category. The patient was started on azacitidine, a hypomethylating agent. A referral to a bone marrow transplant was also done for the consideration of an allogeneic stem cell transplant.
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