Proteasome inhibitor-associated histiocytoid Sweet's syndrome: Clinical and histological similarities to Nakajo-Nishimura syndrome suggest a potential mechanism.

Autor: Cho R; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan., Nakajima S; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.; Department of Drug Discovery for Inflammatory Skin Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan., Kaku Y; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan., Tezuka J; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan., Fujimoto M; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan., Kambe N; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan., Kabashima K; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.; A*STAR Skin Research Labs (A*SRL), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.; Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Jazyk: angličtina
Zdroj: The Journal of dermatology [J Dermatol] 2024 Oct; Vol. 51 (10), pp. 1355-1359. Date of Electronic Publication: 2024 Apr 01.
DOI: 10.1111/1346-8138.17201
Abstrakt: Histiocytoid Sweet's syndrome (HSS) is a variant of Sweet's syndrome (SS) that clinically resembles SS but differs histologically by infiltrates, predominantly composed of immature cells of the myeloid lineage. Medications such as proteasome inhibitors have been reported to cause HSS but there has been little discussion on the underlying mechanism. Here we report two cases of HSS associated with a proteasome inhibitor. Both patients were on ixazomib for the treatment of multiple myeloma and presented with acute erythematous plaques on the upper half of the body. Pathological findings were consistent with HSS. Similarities between proteasome inhibitor-induced HSS and Nakajo-Nishimura syndrome, an inherited inflammatory disease, can be identified both clinically and histologically, suggesting a potential explanation of the mechanism behind proteasome inhibitor-associated HSS.
(© 2024 Japanese Dermatological Association.)
Databáze: MEDLINE
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