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Updated: Mar 18, 2026

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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
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Bevacizumab-induced pityriasis rubra pilaris-like eruption
Shannon Brown1, J Wesley Fletcher1, Katherine H Fiala1
1Department of Dermatology, Baylor Scott & White Health/Texas A&M Health Science Center College of Medicine, Temple, Texas.
Summary
Pityriasis rubra pilaris (PRP) is a rare skin condition. A case report details a patient developing PRP-like symptoms after bevacizumab treatment for macular degeneration, highlighting potential drug-induced reactions.
Area of Science:
- Dermatology
- Ophthalmology
Background:
- Pityriasis rubra pilaris (PRP) is a rare, chronic inflammatory skin disorder.
- Etiologies are poorly understood, with vitamin A deficiency and autoimmune factors hypothesized.
- Medication-induced PRP-like eruptions are exceptionally rare.
Observation:
- A 70-year-old male presented with erythroderma.
- The condition was clinically and histologically consistent with pityriasis rubra pilaris.
- Onset occurred 10 days post-intravitreal bevacizumab injection for age-related macular degeneration.
Findings:
- This is the first reported case of pityriasis rubra pilaris associated with bevacizumab.
- Bevacizumab, an anti-VEGF agent, may trigger PRP-like skin reactions.
- The patient's presentation mimicked classic PRP.
Implications:
- Highlights the importance of recognizing rare adverse drug reactions.
- Clinicians should consider bevacizumab as a potential cause of PRP-like eruptions.
- Further investigation into immune-modulating effects of anti-VEGF therapies is warranted.
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