# Severe 3,4-Methylenedioxymethamphetamine (MDMA)-Associated Rhabdomyolysis in Crohn’s Disease: Direct Toxicity and Inflammatory Susceptibility in the Absence of Hyperthermia

**Authors:** Sebastian Hernandez Mejia, Aishwarya Ashwinee, Ranwa Aldaker

PMC · DOI: 10.7759/cureus.101526 · Cureus · 2026-01-14

## TL;DR

A man with Crohn’s disease developed severe muscle damage from MDMA without high fever, suggesting a new toxicity mechanism unrelated to heat.

## Contribution

Identifies a non-hyperthermic, direct muscle toxicity mechanism of MDMA, possibly worsened by Crohn’s disease.

## Key findings

- MDMA caused severe rhabdomyolysis without hyperthermia or exertion in a patient with Crohn’s disease.
- The case shows the third-highest creatine kinase levels reported in MDMA-related rhabdomyolysis.
- Suggests that Crohn’s disease may increase susceptibility to MDMA-induced muscle injury.

## Abstract

Rhabdomyolysis is a recognized complication of 3,4-methylenedioxymethamphetamine (MDMA), usually driven by severe hyperthermia and agitation. We describe a previously healthy 45-year-old man who developed profound rhabdomyolysis (creatine kinase (CK) 160,000 U/L) and intrinsic acute kidney injury requiring hemodialysis after ingesting 1.5 g of “Molly” (pure MDMA), despite remaining afebrile throughout. In the literature review, the first reported case of severe MDMA-associated rhabdomyolysis without hyperthermia and the third-highest CK values was documented. He later received a new diagnosis of Crohn’s disease, raising the possibility that inflammatory bowel disease-related myositis created an “immune-primed” susceptibility to muscle injury. In contrast to typical MDMA cases, there was no hyperthermia, exertion, serotonin syndrome, or significant electrolyte abnormality to explain the muscle breakdown. This case, therefore, supports an under-recognized, non-hyperthermic mechanism of MDMA toxicity involving direct mitochondrial and oxidative skeletal muscle injury, potentially amplified by occult Crohn’s disease, and highlights the need to consider MDMA toxicity even in afebrile patients presenting with severe rhabdomyolysis.

## Linked entities

- **Chemicals:** 3,4-methylenedioxymethamphetamine (PubChem CID 1615), MDMA (PubChem CID 1615)
- **Diseases:** Crohn’s disease (MONDO:0005011), rhabdomyolysis (MONDO:0005290), acute kidney injury (MONDO:0002492), serotonin syndrome (MONDO:0018546)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** muscle injury (MESH:D009135), inflammatory bowel disease (MESH:D015212), Rhabdomyolysis (MESH:D012206), Toxicity (MESH:D064420), Crohn's Disease (MESH:D003424), agitation (MESH:D011595), myositis (MESH:D009220), acute kidney injury (MESH:D058186), Hyperthermia (MESH:D005334), serotonin (MESH:D020230)
- **Chemicals:** 3,4-Methylenedioxymethamphetamine (MESH:D018817)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12904165/full.md

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Source: https://tomesphere.com/paper/PMC12904165