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Updated: May 2, 2026

The Goeckerman Regimen for the Treatment of Moderate to Severe Psoriasis
Published on: July 11, 2013
Clopidogrel: a possible exacerbating factor for psoriasis
Vikram K Mahajan1, Gayatri Khatri1, Neel Prabha1
1Department of Dermatology, Venereology & Leprosy, Dr. R. P. Govt. Medical College, Kangra (Tanda) - 176001, Himachal Pradesh, India.
Insights
A patient developed palmoplantar pustular psoriasis linked to cardiovascular medications. Stopping these drugs resolved the psoriasis, but re-challenge with clopidogrel triggered it again, suggesting a drug-induced condition.
Area of Science:
- Dermatology
- Cardiology
- Pharmacology
Background:
- Coronary artery disease (CAD) management often involves multiple medications.
- Palmoplantar pustular psoriasis is a chronic inflammatory skin condition.
- Drug-induced dermatoses are a recognized clinical phenomenon.
Observation:
- A 64-year-old male with suspected CAD was treated with diltiazem, atenolol, aspirin, and atorvastatin.
- He subsequently developed palmoplantar pustulosis, progressing to palmoplantar pustular psoriasis.
- Initial treatment adjustments, including stopping atenolol and switching aspirin to clopidogrel, provided no relief.
Findings:
- Discontinuation of all cardiovascular medications led to the resolution of both psoriasis and CAD symptoms.
- Re-administration of oral clopidogrel precipitated the recurrence of skin lesions.
- This suggests a causal link between clopidogrel and the patient's palmoplantar pustular psoriasis.
Implications:
- This case highlights a potential drug-induced psoriasis, specifically linked to clopidogrel.
- It suggests caution when prescribing antiplatelet agents like clopidogrel or ticlopidine to patients with psoriasis and cardiovascular comorbidities.
- Alternative antiplatelet strategies or careful monitoring may be necessary in such cases.
Abstract:
A 64-year-old man developed palmoplantar pustulosis eventuating into palmoplantar pustular psoriasis following treatment with diltiazem, atenolol, aspirin and atorvastatin for suspected coronary artery disease (CAD). Treatment for psoriasis, stopping atenolol and substituting aspirin with clopidogrel did not benefit. Subsequently, he stopped all his drugs and did not develop psoriasis or symptoms/signs of CAD. Re-challenge with oral clopidogrel precipitated his skin lesions. This case has implications for patients having psoriasis and cardiovascular comorbidity where clopidogrel/ticlopidine or aspirin may not be a useful alternative.
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