# Successful Treatment of Posttransplant Refractory Pure Red Cell Aplasia Following Parvovirus B19 Infection

**Authors:** Yousef Ansara, Omar Marouf, Khalil Abualhumos, Mohammed AbuBaha, Hossam Salameh, Huda Saadeddin, Mohammad Al-Sheikh

PMC · DOI: 10.1155/carm/5542026 · Case Reports in Medicine · 2026-02-03

## TL;DR

A kidney transplant patient with anemia caused by parvovirus B19 was successfully treated with IVIG and blood transfusions after initial therapies failed.

## Contribution

This case highlights effective treatment strategies for posttransplant parvovirus B19-induced PRCA in immunocompromised patients.

## Key findings

- IVIG and blood transfusions led to hemoglobin stabilization and reduced viral load in a posttransplant PRCA patient.
- Persistent parvovirus B19 infection was confirmed as the cause of refractory PRCA through PCR testing.
- Tailored immunosuppressive adjustments were necessary to manage complications like pancytopenia and febrile neutropenia.

## Abstract

Pure red cell aplasia (PRCA), a rare cause of anemia limited to the erythroid lineage, is characterized by normocytic normochromic anemia, severe reticulocytopenia, and markedly reduced or absent erythroid precursors in the bone marrow. We report a 44‐year‐old male with end‐stage renal disease (ESRD) secondary to autosomal dominant polycystic kidney disease (ADPKD) who developed refractory PRCA following a live‐donor renal transplant. One month posttransplant, the patient presented with severe, persistent anemia accompanied by fatigue and dyspnea. Initial management included blood transfusions, vitamin B12 supplementation, and adjustments to immunosuppressive therapy due to suspected drug‐induced cytopenia. Bone marrow biopsy confirmed PRCA, and polymerase chain reaction (PCR) revealed a persistently elevated parvovirus B19 infection, a commonly recognized etiology of PRCA in immunocompromised patients. Treatment included intravenous immunoglobulin (IVIG) and frequent blood transfusions. Despite therapy, the patient experienced recurrent anemia, pancytopenia, and febrile neutropenia. Over successive hospitalizations, hematologic improvement was achieved with hemoglobin stabilization and significant viral load reduction. This case underscores the diagnostic and therapeutic complexity of managing parvovirus B19–induced PRCA in posttransplant patients, emphasizing the need for individualized strategies incorporating IVIG, supportive care, and tailored immunosuppressive regimens.

## Linked entities

- **Diseases:** Pure red cell aplasia (MONDO:0001705), end-stage renal disease (MONDO:0004375), autosomal dominant polycystic kidney disease (MONDO:0004691), anemia (MONDO:0002280), pancytopenia (MONDO:0001529)

## Full-text entities

- **Diseases:** febrile neutropenia (MESH:D064147), fatigue (MESH:D005221), cytopenia (MESH:D006402), anemia (MESH:D000740), ADPKD (MESH:D016891), dyspnea (MESH:D004417), Parvovirus B19 Infection (MESH:D016731), PRCA (MESH:D012010), ESRD (MESH:D007676), pancytopenia (MESH:D010198)
- **Chemicals:** vitamin B12 (MESH:D014805)
- **Species:** Human parvovirus B19 (no rank) [taxon 10798], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12865662/full.md

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Source: https://tomesphere.com/paper/PMC12865662