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Successful salvage therapy with cladribine and rituximab for a patient with a relapsed Asian variant of intravascular large B-cell lymphoma

机译:克拉屈滨和利妥昔单抗成功挽救治疗血管内大B细胞淋巴瘤复发的亚洲变异的患者

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The Asian variant of intravascular large B-cell lymphoma (AIVL) is a rare aggressive lymphoma characterized by various clinical symptoms, hemophagocytic syndrome and predominant growth within vessels. We present a 73-year-old man with relapsed AIVL who had been treated with six courses of CHOP regimen. A half year later, he presented with high fever, sweat, dementia and hepatosplenomegaly without lymphadenopathy. A bone marrow biopsy showed prominent hemophagocytosis and immunological staining disclosed an augmented intrasinusal pattern of atypical large lymphocytes characteristic of the CD20+ and CD5+ phenotypes. As salvage therapy, CND-R (rituximab, cladribine, mitoxantrone, dexamethasone) was performed, and the clinical symptoms immediately and dramatically improved. Subsequently, CND-R therapy was repeated every 4 weeks. No serious adverse events were observed with the exception of grade 4 neutropenia and grade 3 thrombocytopenia. After completion of the fifth course, a bone marrow biopsy pathologically confirmed complete remission, leading to termination of this therapy. The patient has remained in remission for more than 15 months. CND-R therapy, which is effective for indolent lymphoma, may be one of the candidates in salvage therapy for relapsed AIVL.
机译:血管内大B细胞淋巴瘤(AIVL)的亚洲变异是一种罕见的侵袭性淋巴瘤,其特征是各种临床症状,噬血细胞综合征和血管内主要生长。我们介绍了一名73岁的AIVL复发患者,他接受了6个疗程的CHOP方案治疗。半年后,他出现高烧,出汗,痴呆和肝脾肿大,无淋巴结肿大。骨髓活检显示出明显的噬血细胞作用,免疫学染色显示具有典型的CD20 +和CD5 +表型的非典型大淋巴细胞的鼻窦内模式增加。作为挽救疗法,进行了CND-R(利妥昔单抗,克拉屈滨,米托蒽醌,地塞米松)治疗,临床症状立即得到显着改善。随后,每4周重复一次CND-R治疗。除4级中性粒细胞减少症和3级血小板减少症外,未观察到严重的不良事件。在完成第五个疗程后,经病理学证实骨髓活检已完全缓解,从而终止了该疗法。该患者已缓解超过15个月。对惰性淋巴瘤有效的CND-R治疗可能是挽救AIVL复发的候选治疗方法之一。

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