# Maculopapular-Type Drug Eruption Caused by Cetuximab

**Authors:** Noriko Ikegawa, Natsuko Saito-Sasaki, Yu Sawada

PMC · DOI: 10.7759/cureus.102768 · Cureus · 2026-02-01

## TL;DR

An 85-year-old woman with colon cancer experienced a delayed skin reaction to cetuximab, suggesting a rare type IV hypersensitivity.

## Contribution

This case report highlights a rare delayed hypersensitivity reaction to cetuximab, expanding understanding of its adverse effects.

## Key findings

- A reproducible maculopapular eruption occurred days after cetuximab re-administration.
- Histopathology showed interface dermatitis and eosinophilic infiltration.
- The clinical and histologic features supported a type IV hypersensitivity diagnosis.

## Abstract

Cetuximab, a chimeric immunoglobulin G1 (IgG1) monoclonal antibody targeting the epidermal growth factor receptor, is well known to cause immediate hypersensitivity reactions mediated by pre-existing IgE antibodies against galactose-α-1,3-galactose (α-gal). In contrast, T-cell-mediated type IV hypersensitivity reactions are exceedingly rare. We report an 85-year-old woman with stage IV colon cancer who developed a reproducible exanthematous (maculopapular) drug eruption after the re-administration of cetuximab. The eruption occurred several days after infusion, resolved promptly after drug discontinuation, and recurred upon unintentional re-exposure during routine oncologic re-administration. Histopathology revealed interface dermatitis with eosinophilic infiltration, and laboratory findings showed mild eosinophilia. The clinical course and histologic features, including a reproducible eruption upon re-exposure, were strongly consistent with a drug-induced type IV hypersensitivity reaction, supporting the diagnosis. This case underscores the importance of recognizing delayed cutaneous adverse reactions when considering treatment interruption and re-challenge during prolonged or intermittent cetuximab therapy.

## Linked entities

- **Diseases:** colon cancer (MONDO:0002032)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, Egfr (epidermal growth factor receptor) [NCBI Gene 13649] {aka 9030024J15Rik, Erbb, Errb1, Errp, Wa5, wa-2}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** stage IV (MESH:D062706), IV (MESH:D006011), drug hypersensitivity (MESH:D004342), type IV (T (MESH:C000631847), cutaneous eruption (MESH:D003875), exanthematous eruption (MESH:D056150), type IV hypersensitivity (MESH:D006968), epidermal necrosis (MESH:D004814), erythematous macules (MESH:C537836), Viral exanthems (MESH:D014777), colon cancer (MESH:D015179), paronychia (MESH:D010304), Paraneoplastic eruptions (MESH:D010257), cutaneous adverse (MESH:D013262), anaphylaxis (MESH:D000707), inflammatory rashes (MESH:D005076), erythematous lesion (MESH:D009059), dermatitis (MESH:D003872), acneiform eruptions (MESH:D017486), cancer (MESH:D009369), colorectal and head-and-neck cancers (MESH:D006258), eosinophilia (MESH:D004802), inflammation (MESH:D007249), hepatic or renal dysfunction (MESH:D008107), skin eruption (MESH:D012871)
- **Chemicals:** fexofenadine (MESH:C093230), Cetuximab (MESH:D000068818), alpha-gal (MESH:C055075), hematoxylin (MESH:D006416)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12954821/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954821/full.md

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Source: https://tomesphere.com/paper/PMC12954821