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- Yoshiki Yamamoto, Asako Mitsui, Kentaro Noda, Yasuo Suzuki, Akihiko Sawaki, Toshihiko Shinoki, Hiroshi Imai, Kana Miyazaki, Isao Tawara, and Ayako Nakajima.
- Center for Rheumatic Diseases, Mie University Hospital, Japan.
- Intern. Med. 2023 May 15; 62 (10): 153715401537-1540.
AbstractSubcutaneous panniculitis-like T cell lymphoma (SPTCL) is a very rare cutaneous T cell lymphoma that has been reported to be associated with autoimmune disorders but is most commonly associated with systemic lupus erythematosus. We herein report a 26-year-old man thought to have lupus panniculitis (LP) treated for 10 years with corticosteroids and cyclosporine. After several relapses with panniculitis, he was finally diagnosed with SPTCL, which was confirmed to have a HAVCR2 mutation for p.Tyr82Cys. We emphasize that rheumatologists should be aware of the possibility of SPTCL, despite its rare appearance, when making a diagnosis of LP or when encountering clinical manifestations that are not consistent with LP.
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