Erlotinib-induced trichomegaly of eyelashes in lung cancer treatment: Epidermal growth factor receptor inhibitor side effect

Dermatol Online J. 2025 Apr 15;31(2). doi: 10.5070/D331265292.

Abstract

Erlotinib is one of the epithelial growth factor receptor tyrosine kinase inhibitors that have been developed and extensively employed in the treatment of non-small cell lung cancer, particularly in individuals with activating epithelial growth factor receptor mutations. This report presents a case of erlotinib induced eyelash trichomegaly and irritation, a rare side effect in a woman who received erlotinib for lung adenocarcinoma. Following the detection of an epithelial growth factor receptor mutation in tumor tissue from a non-small cell lung cancer in a nonsmoking woman, the patient was initiated on erlotinib therapy. After several months, she experienced significant overgrowth of both eyelashes, leading to vision problems. Dermoscopy findings revealed an increase in the length and thickness of the eyelashes associated with inflammation of the eyelid's edges. It has been hypothesized that the inhibition of epithelial growth factor receptor signaling by epithelial growth factor receptor tyrosine kinase inhibitors could alter the growth pattern of hair, potentially leading to the induction of abnormal hair growth, such as trichomegaly, which has been reported only in a small number of case reports.

Publication types

  • Case Reports

MeSH terms

  • Adenocarcinoma / drug therapy
  • Antineoplastic Agents* / adverse effects
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / genetics
  • Erlotinib Hydrochloride* / adverse effects
  • Eyelashes* / drug effects
  • Eyelashes* / growth & development
  • Eyelashes* / pathology
  • Female
  • Humans
  • Hypertrichosis* / chemically induced
  • Lung Neoplasms* / drug therapy
  • Middle Aged
  • Protein Kinase Inhibitors* / adverse effects
  • Protein Kinase Inhibitors* / therapeutic use

Substances

  • Antineoplastic Agents
  • ErbB Receptors
  • Erlotinib Hydrochloride
  • Protein Kinase Inhibitors