Linear IgA bullous dermatosis in association with nodal peripheral T cell lymphoma with a T follicular helper phenotype and multiple myeloma: a case report and literature review
Tempo di lettura: 1 min
Linear IgA bullous dermatosis in association with nodal peripheral T cell lymphoma with a T follicular helper phenotype and multiple myeloma: a case report and literature review.
Abstract
Linear IgA bullous dermatosis (LABD) is a rare autoimmune bullous disease that results in subepidermal blisters with an infiltration of neutrophils and deposition of IgA at the dermo-epidermal junction [1]. It is classified into a paediatric type and adult type. We herein describe an adult case of LABD associated with nodal peripheral T cell lymphoma (PTCL) with a T follicular helper (TFH) phenotype and multiple myeloma. A Japanese male in his 40s with no history of medication developed itchy eruptions [...]
Eur J Dermatol. 2023;33(6):688-689. doi:10.1684/ejd.2023.4553
Linear IgA bullous dermatosis in association with nodal peripheral T cell lymphoma with a T follicular helper phenotype and multiple myeloma: a case report and literature review. Masuda M. et al. IF: 2.5