Abstract: 【Abstract】 Bullous pemphigoid （BP） is an autoimmune subepidermal blistering skin disease that primarily affects the elderly. Clinically, it is characterized by tense blisters and bullae on the local or whole body skin, which can be life-threatening in some patients. The pathogenesis of BP is closely related to anti-BP180 and anti-BP230 antibodies, which cause BP through pathways such as complement activation systems and non-complement systems. This consensus covers clinical characteristics, diagnostic criteria, treatment options, and management of comorbidities associated with BP, with a particular emphasis on the importance of individualized treatment. In terms of diagnosis, a comprehensive approach integrating clinical manifestations, histopathological features, direct immunofluorescence and serological testing results is proposed to improve diagnostic accuracy. In terms of treatment, in addition to traditional glucocorticoids and immunosuppressive agents, new drugs such as biological agents are also recommended, and individualized treatment regimens are formulated according to the disease severity. Additionally, the consensus also pays attention to the management of BP-related comorbidities such as diabetes, kidney disease, and malignant tumors, providing comprehensive guidance for clinicians to improve the treatment outcomes and quality of life of BP patients.

Key words: Pemphigoid, bullous, Diagnosis, Therapeutics, Consensus, Biological agents