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. 2025 Apr;23(4):467-477.
doi: 10.1111/ddg.15625. Epub 2025 Jan 16.

Is Kaposi sarcoma a novel comorbidity of cutaneous lymphoma? A systematic review of the literature

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Is Kaposi sarcoma a novel comorbidity of cutaneous lymphoma? A systematic review of the literature

Rose K C Moritz et al. J Dtsch Dermatol Ges. 2025 Apr.

Abstract

Background and objectives: Patients with cutaneous lymphomas (CL) are at an increased risk of developing secondary malignancies. This study aimed to assess the frequency of association between CL and Kaposi sarcoma (KS) and to identify factors that may promote the co-occurrence of these two diseases.

Patients and methods: On January 25, 2024, we conducted a systematic search of four electronic medical databases to identify all published cases of KS associated with CL. The clinical course and outcomes of these patients were summarized. For critical appraisal, we applied the JBI Checklist for Case Reports. The study was registered in the PROSPERO database (CRD42022313204).

Results: A total of 40 articles reporting on 45 patients were assessed for eligibility. We included 27 cases in the final analysis (26 cutaneous T-cell lymphomas, 1 cutaneous B-cell lymphoma). In 71% of cases, the diagnosis of CL preceded KS. Nearly half (48%) of the patients had erythrodermic mycosis fungoides or Sézary syndrome. KS lesions were predominantly limited to the skin, with complete remission achieved in 53% of cases.

Conclusions: The association between KS and CL is rare, limiting our study due to the small sample size and potential reporting bias. Skin-targeted therapies, a restricted T-cell repertoire, and impaired T-cell responses in erythrodermic CTCL patients may contribute to the development of KS.

Keywords: CBCL; CTCL; Kaposi Sarcoma; Mycosis fungoides; Sézary Syndrome; cutaneous lymphoma.

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Conflict of interest statement

R.K.C.M. has received consultant, speaker fees, and travel support from Kyowa Kirin GmbH, Recordati Rare Diseases, and Takeda Pharmaceutical and has served as a principal investigator in clinical trials conducted by Innate Pharma and 4SC GmbH. J.H. has received speaker fees and travel grants from Bristol Myers Squibb (BMS) and Kyowa Kirin. G.P. has received consultant, speaker fees, or travel grants from BMS, MSD, Novartis, Amgen, and Sun Pharma. R.S. has received research grants, scientific awards, or honoraria for participation in advisory boards, clinical trials, or as a speaker for the following organizations: AbbVie Inc., AbbVie Deutschland GmbH & Co. KG, Almirall Hermal GmbH, Amgen GmbH, Bayer Schering Pharma AG, Boehringer Ingelheim Pharma GmbH & Co. KG, Bruno Bloch Stiftung, Celgene/Bristol Myers Squibb, CSL Behring, Charité Research Organisation GmbH, Flexopharm GmbH & Co. KG, ICON plc, IQVIA RDS GmbH, Incyte Corporation, Janssen‐Cilag GmbH, MoonLake Immunotherapeutics AG, Novartis Pharma GmbH, Parexel International GmbH, Rheinische Friedrich‐Wilhelms‐Universität Bonn, Sanofi‐Aventis Deutschland GmbH, TFS GmbH, UCB Biopharma SPRL, Universitätsmedizin Greifswald, and Wundnetz Berlin‐Brandenburg e.V. M.S. has received consultant, speaker fees, and travel grants from BMS, MSD, Roche, Kyowa Kirin, Novartis, Sanofi Genzyme, Pierre Fabre, Sun Pharma, and Immunocore. G.D. has received consultant, speaker fees, and travel support from Kyowa Kirin, Recordati Rare Diseases, Helsinn, Mallinckrodt Therakos, and Takeda Pharmaceutical.

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