# A Case of Hypoxemic Primary Cytomegalovirus Disease Shortly After Recovery From Coronavirus Disease in a Young Immunocompetent Man

**Authors:** Yoshihiro Kitahara, Kanako Nakamoto, Yusuke Takayama, Kei Miwata, Goki Ushio, Shoshi Akieda, Toshiro Takafuta

PMC · DOI: 10.1155/crdi/7915155 · Case Reports in Infectious Diseases · 2025-10-09

## TL;DR

A young healthy man developed CMV disease with pneumonia and breathing issues shortly after recovering from moderate COVID-19.

## Contribution

Reports of primary CMV disease in young immunocompetent patients after COVID-19 are rare, and this case highlights the need for differential diagnosis.

## Key findings

- Primary CMV disease was diagnosed in a young immunocompetent man after recovery from moderate COVID-19.
- CMV IgM and IgG antibodies became positive during the second admission, indicating a new CMV infection.
- The patient's symptoms improved with ganciclovir treatment, suggesting CMV as the dominant pathogen.

## Abstract

Cytomegalovirus (CMV) reactivation has been identified as a significant predictor of death in patients hospitalized with coronavirus disease (COVID-19). However, reports of concurrent or subsequent primary CMV disease in young immunocompetent patients with COVID-19 are rare. We present a rare case of primary CMV disease manifesting as pneumonia and acute respiratory failure in a young immunocompetent man, which developed shortly after recovery from moderate COVID-19. A 19-year-old immunocompetent man was admitted to our hospital with a diagnosis of COVID-19 pneumonia on the 10th day of COVID-19 onset. His symptoms improved following administration of intravenous dexamethasone, oral prednisolone, and oral azithromycin hydrate and levofloxacin hydrate. He was discharged on the 16th day of COVID-19 onset. However, he developed a cough and fever 5 days after discharge, and he was readmitted to our hospital 8 days after discharge. Serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), C-reactive protein (CRP), and lactate dehydrogenase (LDH) were elevated compared to those during the first admission. Computed tomography revealed new ground-glass attenuations and the improvement in the aforementioned COVID-19 pneumonia. Next day, his percutaneous arterial oxygen saturation levels dropped to 89% breathing room air. Serum antibodies against CMV: immunoglobulin M (CMV IgM) and immunoglobulin G (CMV IgG), which were negative on the day of the first admission, became positive (CMV IgM titer, 5.82 [sample relative light units/cutoff] and CMV IgG titer, 58.6 [arbitrary units/mL]) on the 3rd day of the second admission. The patient was diagnosed with primary CMV disease based on positive test results of the CMV antigenemia and deoxyribonucleic acid of CMV. The patient's symptoms, hypoxemia, and the new ground-glass attenuations improved following intravenous ganciclovir administration, without using corticosteroids. The clinical course in the present case suggests that CMV could have been the dominant causative pathogen for the new pneumonic shadows observed on the second admission. In cases where a second fever occurs shortly after recovery from COVID-19, clinicians should not assume prolonged COVID-19, and primary CMV disease should be considered as a differential diagnosis, even in young immunocompetent patients.

## Linked entities

- **Chemicals:** dexamethasone (PubChem CID 5743), prednisolone (PubChem CID 5755), azithromycin hydrate (PubChem CID 441190), levofloxacin hydrate (PubChem CID 3033924), ganciclovir (PubChem CID 135398740)
- **Diseases:** pneumonia (MONDO:0005249), acute respiratory failure (MONDO:0001208)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** Coronavirus Disease (MESH:D018352), hypoxemia (MESH:D000860), prolonged COVID-19 (MESH:D000094024), death (MESH:D003643), CMV (MESH:D003586), fever (MESH:D005334), respiratory failure (MESH:D012131), cough (MESH:D003371), COVID-19 (MESH:D000086382), pneumonia (MESH:D011014)
- **Chemicals:** levofloxacin (MESH:D064704), oxygen (MESH:D010100), ganciclovir (MESH:D015774), azithromycin (MESH:D017963), dexamethasone (MESH:D003907), prednisolone (MESH:D011239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12566954/full.md

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Source: https://tomesphere.com/paper/PMC12566954