“…However, the rate of grade ≥3 adverse events remains low and treatment discontinuation due to toxicity (Byrd et al , , ) is uncommon and mostly related to infections (Byrd et al , , ; Burger et al , ; Puła et al , ; Tran & O'Brien, ). Dermatological toxicities have also been reported in 2–27% of treated patients (Ransohoff & Kwong, ; Iberri et al , ), mainly mild‐to‐moderate rash, neutrophilic panniculitis, progressive hair and nail changes, skin infections, bruising, petechiae and purpuric eruption (Fabbro et al , ; Bitar et al , ; Ransohoff & Kwong, ; Iberri et al , ). In contrast, oral toxicity with ibrutinib has rarely been described.…”