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风湿性疾病中的卡波西肉瘤。

Kaposi's sarcoma in rheumatic diseases.

作者信息

Louthrenoo Worawit, Kasitanon Nuntana, Mahanuphab Pongsak, Bhoopat Lertlakana, Thongprasert Sumitra

机构信息

Division of Rheumatology, Department of Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Semin Arthritis Rheum. 2003 Apr;32(5):326-33. doi: 10.1053/sarh.2002.50000.

Abstract

OBJECTIVE

To review the clinical features and outcome of all reported cases of Kaposi's sarcoma in patients with rheumatic diseases.

METHODS

In addition to our patient, we identified cases from a Medline search between the years 1966 and 2002. Cases associated with human immunodeficiency virus infection were excluded.

RESULTS

Including our patient, there were a total of 25 cases reported (11 men and 14 women). Rheumatoid arthritis was present in 8 cases, polymyositis/dermatomyositis in 5, vasculitis syndromes in 5, systemic lupus erythematosus in 3, polymyalgia rheumatica in 2, and 1 each of undifferentiated connective tissue disease and Behcet disease. All but 1 patient had been given systemic corticosteroids for a duration that ranged from 6 weeks to 22 years, and immunosuppressive drugs from 25 days to 3.5 years. The Kaposi's lesions usually involved the skin on the extremities; internal organ involvement occurred in 7 cases. Most lesions responded to a decreasing dosage of corticosteroids and immunosuppressive drugs, or to the administration of radiation or cytotoxic therapy. Six patients died, 4 of which were related to the progression of Kaposi's sarcoma.

CONCLUSION

Kaposi's sarcoma in patients with rheumatologic conditions is rare. The clinical features are similar to those with classical Kaposi's sarcoma. Tumor regression usually occurs with decreasing corticosteroids and/or immunosuppressive drugs, local irradiation, or cytotoxic therapy.

摘要

目的

回顾所有已报道的风湿性疾病患者中卡波西肉瘤病例的临床特征及转归。

方法

除了我们的患者外,我们通过检索1966年至2002年间的医学文献数据库(Medline)来确定病例。排除与人类免疫缺陷病毒感染相关的病例。

结果

包括我们的患者在内,共报道了25例(男性11例,女性14例)。其中类风湿关节炎8例,多发性肌炎/皮肌炎5例,血管炎综合征5例,系统性红斑狼疮3例,风湿性多肌痛2例,未分化结缔组织病和白塞病各1例。除1例患者外,所有患者均接受过全身糖皮质激素治疗,疗程为6周至22年,免疫抑制药物治疗时间为25天至3.5年。卡波西肉瘤病变通常累及四肢皮肤;7例出现内脏受累。大多数病变对糖皮质激素和免疫抑制药物剂量减少、或放疗或细胞毒性治疗有反应。6例患者死亡,其中4例与卡波西肉瘤进展有关。

结论

风湿性疾病患者中的卡波西肉瘤罕见。其临床特征与经典卡波西肉瘤相似。肿瘤通常在糖皮质激素和/或免疫抑制药物剂量减少、局部放疗或细胞毒性治疗后消退。

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