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Published on: October 3, 2019
Etoricoxib-induced fixed drug eruption with positive lesional patch tests
Ana Maria Calistru1, Ana Paula Cunha, Ana Nogueira
1Department of Dermatology and Venereology, Hospital São João EPE, Porto, Portugal. anagruia@yahoo.com
Fixed drug eruption (FDE) can be triggered by cyclooxygenase 2 (COX-2) inhibitors like etoricoxib. Patch testing confirmed etoricoxib as the cause of FDE in this case, highlighting potential cutaneous adverse reactions.
Area of Science:
- Dermatology
- Pharmacology
Background:
- Fixed drug eruption (FDE) is a common cutaneous reaction, typically associated with antibiotics, anticonvulsants, and nonsteroidal anti-inflammatory drugs (NSAIDs).
- Cyclooxygenase 2 (COX-2) inhibitors are less frequently implicated in FDE.
- Etoricoxib is a newer COX-2 inhibitor used for pain management.
Observation:
- A 52-year-old woman presented with recurrent, erythematous, pruritic plaques on her neck, forearm, and finger, which healed with hyperpigmentation.
- The lesions consistently reappeared in the same locations after sporadic oral administration of etoricoxib (90 mg) for back pain.
- The time interval between etoricoxib intake and lesion appearance progressively shortened.
Findings:
- Patch tests with etoricoxib (1% and 5% in petrolatum) were positive on lesional skin and negative on nonlesional skin.
- Standard European and NSAID series patch tests were negative.
- Patch tests in 10 healthy controls using etoricoxib were negative, supporting etoricoxib as the causative agent for FDE in this patient.
Implications:
- Patch testing with etoricoxib proved reliable for diagnosing FDE, obviating the need for potentially risky oral provocation tests.
- This case underscores that even drugs considered safe, like etoricoxib, can cause cutaneous adverse reactions, including FDE.
- Clinicians should consider FDE when evaluating patients presenting with recurrent skin lesions potentially linked to COX-2 inhibitor use, especially given the increasing prescription of these agents for pain control.
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