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Cutaneous adverse effects during therapy with an epidermal growth factor receptor (EGFR) inhibitor
Francesca Santoro1, Emanuele Cozzani, Aurora Parodi
1Di.S.E.M. Section of Dermatology, University of Genoa, Italy.
Abstract:
The use of epidermal growth factor receptor (EGFR) inhibitors for the treatment of solid tumours is now increasing. Cutaneous side effects, namely acneiform eruption, xerosis, telangiectasia, hyperpigmentation, fissures, hair and nail changes, are reported in literature. We describe a case of a man treated with an EGFR-inhibitor (erlotinib) for a cell lung cancer who developed skin manifestations localized in an uncommon area and with an atypical evolution.
Insights
Epidermal growth factor receptor (EGFR) inhibitors are increasingly used for solid tumors, but can cause skin side effects. This case highlights uncommon skin reactions to erlotinib in a lung cancer patient.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Epidermal growth factor receptor (EGFR) inhibitors are a growing class of targeted therapies for solid tumors.
- Cutaneous side effects are common with EGFR inhibitors, including acneiform eruptions, xerosis, and nail changes.
Observation:
- A case study of a male patient with non-small cell lung cancer treated with erlotinib.
- The patient developed unusual skin manifestations in an uncommon body area.
- The skin condition exhibited an atypical progression and presentation.
Findings:
- The patient experienced localized and atypical skin side effects during erlotinib therapy.
- This presentation differs from commonly reported cutaneous adverse events associated with EGFR inhibitors.
Implications:
- Highlights the need for awareness of diverse and uncommon skin toxicities from EGFR inhibitors.
- Suggests that clinicians should monitor for atypical dermatological presentations in patients receiving erlotinib.
- Contributes to understanding the full spectrum of erlotinib-induced skin reactions.
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