Pembrolizumab-Induced Bullous Pemphigoid
Navigating Diagnostic Challenges and Treatment Resistance.
Moeckel C, Ferguson S
CutisIn the feed 24 Jul 2026, issue 2026 May, added to PubMed 24 Jul 2026
Topics: Autoimmune & connective tissueDrug reactionsDermatopathologyCancer drugs
Abstract
Immune checkpoint inhibitors (ICIs), including the programmed cell death protein-1 (PD-1) inhibitor pembrolizumab, have revolutionized metastatic urothelial carcinoma management but are frequently associated with cutaneous immune-related adverse events, including drug-induced bullous pemphigoid (DIBP). We present the case of an 81-year-old man with PD-L1-negative metastatic high-grade papillary urothelial carcinoma with a generalized, pruritic, bullous eruption following treatment with pembrolizumab. Histopathology and direct immunofluorescence confirmed bullous pemphigoid (BP). This case underscores the diagnostic challenges of DIBP. Clinicians must maintain a high index of suspicion and consider early transition to steroid-sparing agents such as rituximab in refractory cases. Timely dermatologic referral and close multidisciplinary coordination are essential.
Abstract from PubMed
PMID 42497339 · DOI 10.12788/cutis.1411