Lokare Anand, Nikolousis Emmanouil, Phillips Neil, Rudzki Zbigniew, Lovell Richard, Kishore Bhuvan, Milligan Don, Paneesha Shankara
Hematology Department, University Hospital Walsgrave , Coventry, UK.
Hematology Department, Heart of England Hospital NHS Trust , Birmingham, UK.
Hematol Rep. 2014 Jan 29;6(1):5119. doi: 10.4081/hr.2014.5119.
Blastic plasmacytoid dendritic cell neoplasm is a rare, aggressive tumor characterized by skin and/or marrow infiltration by CD4(+) CD56(+) cells. Historically, the tumor was variably thought to arise from either monocytes, T cells or NK cells giving rise to terms such as CD4(+)/CD56(+) acute monoblastic leukemia, primary cutaneous CD4(+)/CD56(+) hematodermic tumor and blastic NK-cell lymphoma. Whilst considerable progress has been made in understanding the histogenesis, the best modality of treatment remains to be defined. We are therefore reporting this case which was successfully treated with a T-deplete allogeneic transplant and the patient is currently alive and in remission 4 years post transplant.
母细胞性浆细胞样树突状细胞肿瘤是一种罕见的侵袭性肿瘤,其特征是CD4(+)CD56(+)细胞浸润皮肤和/或骨髓。从历史上看,该肿瘤曾被认为起源于单核细胞、T细胞或NK细胞,从而产生了诸如CD4(+)/CD56(+)急性单核母细胞白血病、原发性皮肤CD4(+)/CD56(+)皮肤肿瘤和母细胞性NK细胞淋巴瘤等术语。虽然在理解其组织发生方面已经取得了相当大的进展,但最佳治疗方式仍有待确定。因此,我们报告该病例,该病例通过去除T细胞的异基因移植成功治疗,患者目前存活,移植后4年处于缓解状态。