Serio B, Giudice V, D'Addona M, Guariglia R, Gorrese M, Bertolini A, D'Alto F, Cuffa B, Pellegrino D, Langella M, Selleri C
Hematology and Transplant Center, University Hospital "San Giovanni di Dio e Ruggi D'Aragona", Italy.
Clinical Pharmacology, University Hospital "San Giovanni di Dio e Ruggi D'Aragona", Italy.
Transl Med UniSa. 2020 Oct 31;23:63-66. doi: 10.37825/2239-9747.1012. eCollection 2020 Oct.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN), an extremely rare and aggressive tumor, derives from plasmacytoid dendritic cell precursors and is characterized by CD4 and CD56 positivity accompanied by the expression of isolated myeloid, B- or T-cell lineage markers. Despite the recent introduction of specific targeted therapies, prognosis is still poor with a median overall survival of one year, and allogeneic bone marrow transplantation remains the only curative treatment in eligible patients. In this series, we described two cases of adult BPDCN treated with high dose cytarabine and methotrexate and autologous hematopoietic stem cell transplantation, or fludarabine, cytarabine, and idarubicin achieving the first a complete lasting remission, while the second only a transient improvement in skin lesions.
母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种极其罕见且侵袭性强的肿瘤,起源于浆细胞样树突状细胞前体,其特征为CD4和CD56阳性,并伴有孤立的髓系、B或T细胞谱系标志物的表达。尽管最近引入了特异性靶向治疗,但预后仍然很差,中位总生存期为一年,异基因骨髓移植仍然是符合条件患者的唯一治愈性治疗方法。在本系列中,我们描述了两例成人BPDCN患者,一例接受大剂量阿糖胞苷和甲氨蝶呤以及自体造血干细胞移植治疗,另一例接受氟达拉滨、阿糖胞苷和伊达比星治疗,第一例实现了完全持久缓解,而第二例仅皮肤病变有短暂改善。