# Imatinib-induced rhabdomyolysis: A case report

**Authors:** Jordan Rubenstein, Sarah M. Schwartz, Jay Vankawala, Michael Caplan, Steven Shea, Joseph G. Jurcic

PMC · DOI: 10.1016/j.lrr.2026.100561 · Leukemia Research Reports · 2026-01-12

## TL;DR

An elderly woman developed severe muscle damage from imatinib, a cancer drug, but recovered after stopping the medication.

## Contribution

This case report highlights a rare but severe side effect of imatinib and emphasizes the importance of early recognition.

## Key findings

- The patient had CK levels over 24,000 U/L and acute kidney injury linked to imatinib.
- Discontinuation of imatinib led to rapid normalization of CK and kidney function.
- MRI showed muscle and fascial edema consistent with rhabdomyolysis.

## Abstract

Imatinib, a tyrosine kinase inhibitor used for chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST), is associated with myalgia and creatine kinase (CK) elevations, though severe rhabdomyolysis and myopathy are rare. We report an 83-year-old woman with CML who developed progressive proximal weakness, dark urine, and acute kidney injury after three years of imatinib therapy. Laboratory evaluation revealed CK >24,000 U/L, transaminitis, and myoglobinuria. MRI showed diffuse muscle and fascial edema, while autoimmune testing was negative. Imatinib and rosuvastatin were discontinued, and the patient was managed with intravenous fluids and supportive care. CK and renal function normalized within 10 days, with substantial recovery of strength. The strong temporal relationship between drug withdrawal and improvement implicates imatinib as the etiology. This case represents one of the most severe reported instances of imatinib-induced rhabdomyolysis. Early recognition and discontinuation are essential to prevent life-threatening sequelae.

## Linked entities

- **Chemicals:** imatinib (PubChem CID 5291), rosuvastatin (PubChem CID 446157)
- **Diseases:** chronic myeloid leukemia (MONDO:0011996), rhabdomyolysis (MONDO:0005290), myopathy (MONDO:0005336), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}
- **Diseases:** myoglobinuria (MESH:D009212), CML (MESH:D015464), weakness (MESH:D018908), myopathy (MESH:D009135), GIST (MESH:D046152), muscle and fascial edema (MESH:C563219), myalgia (MESH:D063806), rhabdomyolysis (MESH:D012206), acute kidney injury (MESH:D058186), autoimmune (MESH:D001327)
- **Chemicals:** rosuvastatin (MESH:D000068718), Imatinib (MESH:D000068877)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12830313/full.md

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Source: https://tomesphere.com/paper/PMC12830313