Department of Dermatology, University of Wisconsin, Madison.
Department of Dermatology, University of California, San Francisco3Department of Pathology, University of California, San Francisco.
JAMA Dermatol. 2014 Jan;150(1):73-6. doi: 10.1001/jamadermatol.2013.7141.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare malignant neoplasm with cutaneous manifestations and a rapidly progressive clinical course. The diagnosis relies on characteristic clinicopathologic and immunopathologic features. However, the overlap of immunophenotypic features with other cancers, as well as newly discovered interpersonal and intrapersonal phenotypic variations, renders the identification of BPDCN challenging. A greater understanding of the proteins expressed by BPDCN might facilitate its recognition and provide insights into its clinical behavior.
In 7 of 9 patients at 4 tertiary care institutions, immunohistochemical analysis demonstrated strong CD31/PECAM-1 (platelet endothelial cell adhesion molecule 1) expression by neoplastic cells. Combined with similar findings observed in 1 former patient, 8 of 10 cases of BPDCN were CD31/PECAM-1 positive.
Expression of CD31/PECAM-1 by BPDCN adds new information about the antigenic profile of this unusual neoplasm. CD31/PECAM-1 influences multiple cell functions including adhesion, apoptosis, coagulation, host response, and protein synthesis that might affect clinical features of BPDCN such as hemorrhage, aggressive tumor growth, and resistance to therapy. Therefore, the potential role of this molecule in the tumor formation and progression of BPDCN warrants additional exploration.
原始细胞性浆细胞样树突细胞肿瘤(BPDCN)是一种罕见的恶性肿瘤,具有皮肤表现和快速进展的临床过程。诊断依赖于特征性的临床病理和免疫病理特征。然而,免疫表型特征与其他癌症的重叠,以及新发现的人际和个体内表型变异,使得 BPDCN 的识别具有挑战性。对 BPDCN 表达的蛋白质有更深入的了解可能有助于其识别,并深入了解其临床行为。
在 4 家三级保健机构的 9 名患者中的 7 名患者中,免疫组织化学分析显示肿瘤细胞强烈表达 CD31/PECAM-1(血小板内皮细胞黏附分子 1)。结合在 1 名前患者中观察到的类似发现,10 例 BPDCN 中有 8 例 CD31/PECAM-1 阳性。
BPDCN 中 CD31/PECAM-1 的表达增加了有关这种不寻常肿瘤抗原谱的新信息。CD31/PECAM-1 影响多种细胞功能,包括黏附、凋亡、凝血、宿主反应和蛋白质合成,这些功能可能影响 BPDCN 的临床特征,如出血、侵袭性肿瘤生长和对治疗的抵抗。因此,该分子在 BPDCN 肿瘤形成和进展中的潜在作用值得进一步探索。