Two for two: Dual therapy with erlotinib and acitretin for twins with severe keratoderma in Olmsted syndrome.
Sneha ButalaSheshanna PhanDawn H SiegelValerie CarlbergAmy S PallerPublished in: Pediatric dermatology (2023)
Olmsted syndrome (OS) is a rare genetic disorder, characterized by painful palmoplantar keratoderma (PPK), periorificial and intertriginous hyperkeratoses, and alopecia. Fewer than 75 cases have been described. Variants in TRPV3 result in constitutive activation of transient receptor potential vanilloid 3, leading to increased epidermal growth factor receptor (EGFR) signaling, palmoplantar epidermal hyperproliferation, and exquisite lesional pain. We describe pre-school aged twins with OS with partial improvement from oral erlotinib, an EGFR inhibitor, but dramatic reduction of their persistent palmoplantar thickening and pain from adding acitretin.
Keyphrases
- epidermal growth factor receptor
- advanced non small cell lung cancer
- tyrosine kinase
- chronic pain
- neuropathic pain
- pain management
- copy number
- case report
- physical activity
- gestational age
- small cell lung cancer
- genome wide
- spinal cord
- gene expression
- stem cells
- spinal cord injury
- mesenchymal stem cells
- risk assessment
- cell therapy
- dna methylation
- blood brain barrier
- postoperative pain
- subarachnoid hemorrhage