# Case Report: Immune checkpoint inhibitor-induced myositis without elevated creatine kinase

**Authors:** Klajdi Begaj, Raphael Wilhelm, Alisa Lepper, Maike Kaufhold, Jakob Veeser, Stephan Grabbe, Henner Stege

PMC · DOI: 10.3389/fimmu.2025.1592385 · Frontiers in Immunology · 2025-06-25

## TL;DR

A patient with melanoma developed myositis from cancer treatment, but her muscle enzyme levels stayed normal, highlighting the need for careful diagnosis.

## Contribution

This case report highlights an atypical presentation of ICI-induced myositis with normal creatine kinase levels.

## Key findings

- A 58-year-old female developed ICI-induced myositis without elevated creatine kinase.
- Diagnosis relied on neurological exams, MRI, and electromyography.
- The patient improved with corticosteroids and had no relapse after treatment.

## Abstract

Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of advanced cancers like malignant melanoma. However, they can lead to a range of immune-related adverse events (irAEs), impacting various organ systems. Among these, myositis is a rare but serious irAE, typically characterized by myalgia, muscle weakness, and elevated creatine kinase (CK) levels. Herein, we report the case of a 58-year-old female with advanced melanoma, who presented a delayed-onset of ICI-induced myositis accompanied by severe muscle weakness. Interestingly, the CK levels remained normal throughout her disease course. Neurological examination, MRI, and electromyography were pivotal in diagnosing myositis. Differential diagnoses, including myasthenia gravis, myocarditis, and paraneoplastic syndromes or idiopathic inflammatory myopathies, were systematically ruled out through clinical evaluation, serological testing, and imaging. The patient responded favorably to high-dose corticosteroid therapy, leading to a gradual improvement of symptoms and no relapse after stopping treatment. This case report emphasizes a multimodal diagnostic approach and underscores the importance of clinical awareness for such atypical irAE presentations.

## Linked entities

- **Diseases:** malignant melanoma (MONDO:0005105), myasthenia gravis (MONDO:0009688), myocarditis (MONDO:0004496), idiopathic inflammatory myopathies (MONDO:0020122)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** muscle weakness (MESH:D018908), myasthenia gravis (MESH:D009157), malignant melanoma (MESH:D008545), inflammatory myopathies (MESH:D009220), myalgia (MESH:D063806), paraneoplastic syndromes (MESH:D010257), cancers (MESH:D009369), myocarditis (MESH:D009205)
- **Chemicals:** Immune (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12237670/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12237670/full.md

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Source: https://tomesphere.com/paper/PMC12237670