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

IF 5.5 4区 医学 Q1 DERMATOLOGY Journal Der Deutschen Dermatologischen Gesellschaft Pub Date : 2025-01-16 DOI:10.1111/ddg.15625
Rose K C Moritz, Julia Huynh, Gabriela Poch, Robert Sabat, Max Schlaak, Gabor Dobos
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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.

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卡波西肉瘤是皮肤淋巴瘤的一种新的合并症吗?对文献的系统回顾。
背景和目的:皮肤淋巴瘤(CL)患者发生继发性恶性肿瘤的风险增加。本研究旨在评估CL和卡波西肉瘤(KS)之间的关联频率,并确定可能促进这两种疾病共同发生的因素。患者和方法:2024年1月25日,我们对四个电子医学数据库进行了系统检索,以确定所有已发表的KS合并CL的病例。总结这些患者的临床过程和预后。对于关键的评估,我们应用了案例报告的JBI检查表。该研究已在PROSPERO数据库中注册(CRD42022313204)。结果:共有40篇报道了45例患者的文章被评估为合格。我们最终分析了27例(26例皮肤t细胞淋巴瘤,1例皮肤b细胞淋巴瘤)。在71%的病例中,CL的诊断先于KS。近一半(48%)的患者有红皮病蕈样病或ssamzary综合征。KS病变主要局限于皮肤,53%的病例完全缓解。结论:KS和CL之间的关联是罕见的,由于样本量小和潜在的报告偏倚,限制了我们的研究。红皮病CTCL患者的皮肤靶向治疗、受限的t细胞库和受损的t细胞反应可能有助于KS的发展。
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来源期刊
CiteScore
3.50
自引率
25.00%
发文量
406
审稿时长
1 months
期刊介绍: The JDDG publishes scientific papers from a wide range of disciplines, such as dermatovenereology, allergology, phlebology, dermatosurgery, dermatooncology, and dermatohistopathology. Also in JDDG: information on medical training, continuing education, a calendar of events, book reviews and society announcements. Papers can be submitted in German or English language. In the print version, all articles are published in German. In the online version, all key articles are published in English.
期刊最新文献
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