# Invasive Pulmonary Aspergillosis in a Young Adult With Hyperimmunoglobulin E Syndrome and Hypogammaglobulinemia Following Rituximab Therapy

**Authors:** Gautam K Pandrangi, Ritika N Golechha, Logan R Mills, John T Brown, Nicholas Helmstetter

PMC · DOI: 10.7759/cureus.102562 · Cureus · 2026-01-29

## TL;DR

A young adult with a rare immune disorder and low antibody levels developed a severe fungal lung infection after treatment for lymphoma.

## Contribution

This case highlights the risk of invasive aspergillosis in HIES patients with hypogammaglobulinemia following rituximab therapy.

## Key findings

- The patient's respiratory decline was due to invasive pulmonary aspergillosis, not bacterial infection.
- Rituximab-induced hypogammaglobulinemia increased the risk of opportunistic fungal infections in this HIES patient.
- Early fungal testing is critical in immunocompromised patients with worsening symptoms despite antibiotics.

## Abstract

Hyperimmunoglobulin E syndrome (HIES) is a rare primary immunodeficiency marked by elevated IgE levels, recurrent skin and pulmonary infections, and immune dysregulation. While typically diagnosed in childhood, adult presentations can occur, often complicated by structural lung disease, opportunistic infections, and malignancies. We report a 37-year-old female with signal transducer and activator of transcription 3 (STAT3)-deficient HIES, diffuse large B-cell lymphoma (DLBCL) in remission, rituximab-induced hypogammaglobulinemia, and recurrent infections, who presented with acute-on-chronic dyspnea. Imaging revealed a large cavitary lesion in the left upper lobe. Despite 30 days of appropriate antibiotics targeting methicillin-resistant Staphylococcus aureus (MRSA) and gram-negative organisms, her respiratory status deteriorated, necessitating intubation. Subsequent bronchoalveolar lavage and serum galactomannan testing confirmed invasive pulmonary aspergillosis (IPA) as the etiology of her deterioration, prompting combination antifungal therapy. This case highlights the importance of maintaining a broad differential diagnosis in immunocompromised patients with worsening respiratory symptoms despite antibiotics. Early consideration and testing for fungal infections in high-risk populations can prevent diagnostic delay and improve outcomes.

## Linked entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774]
- **Diseases:** Hyperimmunoglobulin E syndrome (MONDO:0018037), diffuse large B-cell lymphoma (MONDO:0018905)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}
- **Diseases:** arthralgias (MESH:D018771), immune dysfunction (MESH:D007154), primary (MESH:D010538), necrotizing pneumonia (MESH:D000071067), Infections (MESH:D007239), bronchiectasis (MESH:D001987), immunodeficiency (MESH:D007153), Infectious Diseases (MESH:D003141), invasive (MESH:D009361), HIES (MESH:D007589), MRSA (MESH:D013203), lung abscess (MESH:D008169), DLBCL (MESH:D016403), immune dysregulation (OMIM:614878), invasive fungal disease (MESH:D000072742), fungal (MESH:D009181), Aspergillosis (MESH:D001228), myalgias (MESH:D063806), allergy (MESH:D004342), IPA (MESH:D055744), bacterial infections (MESH:D001424), lymphomas (MESH:D008223), Serratia (MESH:D016868), pulmonary injury (MESH:D055370), Klebsiella (MESH:D007710), lung abnormalities (MESH:D008171), opportunistic infections (MESH:D009894), Cancer (MESH:D009369), dyspnea (MESH:D004417), Pulmonary Aspergillosis (MESH:D055732), critically ill (MESH:D016638), Pneumocystis jirovecii (MESH:D011020), pulmonary infections (MESH:D012141), multisystem disease (MESH:D004194), acute hypoxic (MESH:D000208), primary immunodeficiencies (MESH:D000081207), STAT3-deficient (MESH:C566796), bacterial pneumonia (MESH:D018410), pneumonia (MESH:D011014), staphylococcal (MESH:D011023), Hypogammaglobulinemia (MESH:D000361), fungal superinfection (MESH:D015163), urticaria (MESH:D014581), hypoxemic respiratory failure (MESH:D012131), Cavitary Lesion (MESH:C566924)
- **Chemicals:** linezolid (MESH:D000069349), Rituximab (MESH:D000069283), amphotericin B (MESH:D000666), isavuconazole (MESH:C508735), R-CHOP (-), trimethoprim-sulfamethoxazole (MESH:D015662), triazoles (MESH:D014230), galactomannan (MESH:C012990), micafungin (MESH:D000077551), oxygen (MESH:D010100), dapsone (MESH:D003622), methicillin (MESH:D008712), voriconazole (MESH:D065819), echinocandin (MESH:D054714), levofloxacin (MESH:D064704), cefepime (MESH:D000077723), vancomycin (MESH:D014640), atovaquone (MESH:D053626), ertapenem (MESH:D000077727)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773], Staphylococcus aureus (species) [taxon 1280], Aspergillus (genus) [taxon 5052], Klebsiella aerogenes (species) [taxon 548], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949603/full.md

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Source: https://tomesphere.com/paper/PMC12949603