Cladribine chemotherapy of multifocal, multisystemic form of Rosai–Dorfman disease: literature review and case report

V. Potapenko, D. Abramov, V. V. Baykov, T. L. Grigorieva, M. S. Selinkina, L. O. Nikolskaya, Jean-François Emile
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引用次数: 0

Abstract

Rosai–Dorfman disease is the most frequent variant of non-Langerhans cell histiocytosis. Local forms can be resected or irradiated. If the process involves multiple organs, systemic chemotherapy can cure some patients. This article includes literature review and a case report of a 34-year-old patient with multifocal, multisystemic form of Rosai–Dorfman disease with bone and pleural involvement. The diagnosis was based on histological, immunohistochemical, and molecular studies of tumor tissue. Since November 2021, 6 courses of chemotherapy with cladribine and 8 infusions of zolendronic acid were carried out with achievement of durable remission. The tolerance was acceptable.
罗赛-多夫曼病多灶、多系统形式的克拉利宾化疗:文献综述和病例报告
罗赛-多夫曼病是非朗格汉斯细胞组织细胞增生症最常见的变种。局部病变可以切除或照射。如果病变累及多个器官,全身化疗可以治愈部分患者。本文包括文献综述和一例 34 岁患者的病例报告,该患者患有多灶、多系统形式的罗赛-多夫曼病,并累及骨骼和胸膜。诊断基于肿瘤组织的组织学、免疫组化和分子研究。自 2021 年 11 月以来,患者接受了 6 个疗程的克拉利宾化疗和 8 次唑仑膦酸输注,病情得到了持久缓解。耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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