Background Chimeric antigen receptor T-cell therapy targeting B-cell maturation antigen (BCMA CAR-T) has significantly improved outcomes in relapsed/refractory multiple myeloma (R/RMM), yet its spectrum of immune-related adverse events continues to be defined. Among these, cutaneous toxicities are not unusual, but frequently receive insufficient attention. Delayed-onset cutaneous reactions, in particular, may be underreported. Case report We report a patient with R/RMM who achieved stringent complete response (sCR) following BCMA CAR-T therapy and developed delayed-onset cutaneous lesions on day 50 post-infusion. Histopathology revealed dense dermal neutrophilic infiltration, consistent with Sweet’s syndrome. However, the patient lacked typical clinical features such as fever, arthralgia, or peripheral neutrophilia, prompting a diagnosis of ‘Sweet-like syndrome’ associated with CAR-T therapy. The lesions resolved spontaneously without systemic glucocorticoid therapy. Conclusion To our knowledge, virtually no cases of Sweet’s syndrome or Sweet−like syndrome have been reported previously after BCMA CAR−T therapy, broadening the recognized spectrum of CAR−T−related cutaneous adverse events and underscoring the importance of early biopsy for atypical, delayed−onset rashes—rather than empiric systemic corticosteroid treatment—to guide appropriate management.
Ouyang et al. (Thu,) studied this question.