B Serio, V Giudice, M D'Addona, R Guariglia, M Gorrese, A Bertolini, F D'Alto, B Cuffa, D Pellegrino, M Langella, C Selleri
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引用次数: 0
摘要
浆细胞性树突状细胞瘤(BPDCN)是一种极其罕见的侵袭性肿瘤,源于浆细胞性树突状细胞前体,其特征是 CD4 和 CD56 阳性,并伴有孤立的髓系、B 系或 T 系标志物的表达。尽管最近引入了特异性靶向疗法,但预后仍然很差,中位总生存期仅为一年,异基因骨髓移植仍然是符合条件的患者唯一的根治性治疗方法。在这组病例中,我们描述了两例成人BPDCN患者,前者接受大剂量阿糖胞苷、甲氨蝶呤和自体造血干细胞移植,或氟达拉滨、阿糖胞苷和伊达比星治疗后获得完全持久缓解,而后者仅皮肤病变得到短暂改善。
A Case Series of Blastic Plasmacytoid Dendritic Cell Neoplasia.
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.