Saeed Hayder, Awasthi Mukta, Al-Qaisi Abeer, Massarweh Suleiman
Department of Internal Medicine, University of Kentucky , Lexington, KY, USA.
Rare Tumors. 2014 Oct 27;6(4):5474. doi: 10.4081/rt.2014.5474.
Blastic plasmacytoid dendritic neoplasm is an exceedingly rare tumor that has undergone several changes in nomenclature over the last two decades, largely because of confusion regarding its cell of origin. It does, however, have distinctive clinical features with a particularly aggressive clinical course and no standard treatment. Overall, prognosis is poor and relapse is routine after initial response to chemotherapy. In this report, we describe a typical patient with this disease and reconcile the available literature and its evolution. We emphasize the leukemic nature of this tumor's behavior, with extensive central nervous system and skin involvement, and describe for the first time a potential role for maintenance chemotherapy in its treatment.
母细胞性浆细胞样树突状细胞肿瘤是一种极其罕见的肿瘤,在过去二十年中其命名经历了几次变化,主要是因为对其细胞起源存在混淆。然而,它确实具有独特的临床特征,临床病程特别侵袭性且没有标准治疗方法。总体而言,预后很差,对化疗的初始反应后复发很常见。在本报告中,我们描述了一名患有这种疾病的典型患者,并梳理了现有文献及其演变。我们强调了这种肿瘤行为的白血病性质,伴有广泛的中枢神经系统和皮肤受累,并首次描述了维持化疗在其治疗中的潜在作用。