LAUSR

A 78-year-old woman was diagnosed with stage IV A left lower lobe adenocarcinoma by chest computed tomography. There was no history of psoriasis. Her tumor proportion score on PD-L1 was 55%, and she was given Pembrolizumab at 200 mg/body every 3 weeks. After three cycles of treatment, psoriasis-like rashes accompanied by itching rapidly appeared across her body (Picture 1). A skin biopsy indicated psoriasiform dermatitis (Picture 2). In the histopathological findings, the epidermis showed hyperkeratosis with the aggregation of neutrophils (Munro’s microabscess) in the horny cell layer and thickening with regular elongation of rete ridges. She started administration of a topical application of steroid ointment, but her symptoms continued to worsen. Oral steroid tablets (prednisolone 1 mg/kg) were started in order to manage psoriasiform dermatitis as a grade 3 immune-related adverse event (irAE). After the treatment, her psoriasiform dermatitis gradually improved. We were able to gradually reduce the prednisolone without exacerbating the skin rash and finally maintained the dose at 2.5 mg per day (Picture 3). We were considering the re-