Irimia Ruxandra, Barbu Sinziana, Popa Codruta, Badelita Sorina
School of Medicine, "Carol Davila" University of Medicine and Pharmacy, 4192910 Bucharest, Romania.
Fundeni Clinical Institute, 4192910 Bucharest, Romania.
Hematol Rep. 2023 Mar 22;15(1):220-224. doi: 10.3390/hematolrep15010023.
Recently, Brentuximab Vedotin (BV) has emerged as an important therapy not only for Hodgkin's Lymphoma, but also for CD30-positive T cell lymphomas. Although anemia and thrombocytopenia are common myelosuppressive side effects, to our knowledge, this is the first described case of Evans Syndrome associated with BV therapy. We present the case of a 64-year-old female, diagnosed with relapsed Peripheral T Cell Lymphoma Not Otherwise Specified (PTCL-NOS), who, after receiving six cycles of BV, developed authentic severe autoimmune hemolytic anemia with strong positive direct anti-globulin (Coombs) test, simultaneously associated with severe immune thrombocytopenia. The patient was unresponsive to systemic corticotherapy, but fully recovered after a course of IV immunoglobulin.
最近,维布妥昔单抗(BV)不仅已成为霍奇金淋巴瘤的重要治疗方法,也是治疗CD30阳性T细胞淋巴瘤的重要方法。虽然贫血和血小板减少是常见的骨髓抑制副作用,但据我们所知,这是首例报道的与BV治疗相关的伊文氏综合征病例。我们报告了一名64岁女性的病例,该患者被诊断为复发的外周T细胞淋巴瘤,非特指型(PTCL-NOS),在接受六个周期的BV治疗后,出现了严重的自身免疫性溶血性贫血,直接抗球蛋白(库姆斯)试验呈强阳性,同时伴有严重免疫性血小板减少。该患者对全身皮质激素治疗无反应,但在接受一个疗程的静脉注射免疫球蛋白后完全康复。