Awasthi Namrata Punit, Qayoom Sumaira, Dabadghao Sunil
Department of Pathology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.
J Cancer Res Ther. 2017 Oct-Dec;13(6):1056-1058. doi: 10.4103/0973-1482.220358.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy, recognized as a distinct entity in the WHO 2008 classification of hematolymphoid neoplasm. Described for the first time in 1994 as CD4+ cutaneous lymphoma with high expression of CD56, BPDCN has been known previously with various names such as blastic natural killer (NK) leukemia/lymphoma, agranular CD4+ CD56+ hematodermic neoplasm, and agranular CD4+ NK cell leukemia. This disease usually presents with cutaneous involvement as the first manifestation, with subsequent or simultaneous spread to bone marrow and peripheral blood. Leukemia as the first presenting symptom without any cutaneous involvement is a rare finding and can masquerade as acute undifferentiated leukemia. We present here such a case of a 59-year-old male who presented as leukemia without any cutaneous lesion but subsequently developed a scalp nodule.
母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种罕见的血液系统恶性肿瘤,在世界卫生组织2008年血液淋巴系统肿瘤分类中被确认为一种独特的实体。BPDCN于1994年首次被描述为具有CD56高表达的CD4 +皮肤淋巴瘤,此前曾有多种名称,如母细胞性自然杀伤(NK)白血病/淋巴瘤、无颗粒CD4 + CD56 +皮肤肿瘤和无颗粒CD4 + NK细胞白血病。这种疾病通常以皮肤受累为首发表现,随后或同时扩散至骨髓和外周血。以白血病为首发症状且无任何皮肤受累的情况较为罕见,可能会被误诊为急性未分化白血病。我们在此报告一例59岁男性患者,该患者最初表现为白血病且无任何皮肤病变,但随后出现了头皮结节。