母细胞性浆细胞样树突细胞肿瘤临床病理特征分析  

Analysis of clinicopathological features of blastic plasmacytoid dendritic cell neoplasm and literature review

作　　者：李春艳 方雅兰 刘国荣[1] 常丽君 陈少红[1] 丁文双[1] LI Chunyan;FANG Yalan;LIU Guorong;CHANG Lijun;CHEN Shaohong;DING Wenshuang(Department of Pathology,Guangzhou First People s Hospital,School of Medicine,South China University of Technology,Guangzhou 510180,China;Department of Pathology,Affiliated Maoming Hospital of Southern Medical University,Maoming 525000,China;Department of Pathology,Zhuhai Center for Maternal and Child Health Care,Zhuhai 519000,China)

机构地区：[1]广州市第一人民医院,华南理工大学第二附属医院病理科,广州510180 [2]南方医科大学附属茂名医院病理科,茂名525000 [3]珠海市妇幼保健院病理科,珠海519000

出　　处：《广州医药》2023年第3期30-34,共5页Guangzhou Medical Journal

摘　　要：目的学习母细胞性浆细胞样树突细胞肿瘤(BPDCN)的临床病理及免疫表型特征,总结该少见肿瘤的病理诊断经验。方法回顾分析2例BPDCN患者临床资料,通过苏木素-伊红(HE)染色分析肿瘤组织及细胞形态,通过免疫组织化学染色分析肿瘤免疫表型,通过流式细胞学检测骨髓有无肿瘤侵犯,并结合文献分析。结果本报道中1例为97岁女性,临床以皮肤瘀斑结节为首发症状,肿瘤细胞真皮内弥漫浸润,不侵犯表皮,细胞中等大小,核形不规则,核仁不明显。另1例为69岁男性,临床以淋巴结肿大为首发症状,淋巴结结构完全破坏,肿瘤细胞弥漫浸润,细胞呈中等大小的母细胞样,核仁明显。2例免疫表型均表达CD123、CD4、CD56、TDT,不表达B系、T系淋巴细胞及髓系标志物,肿瘤均累及骨髓。结论BPDCN是一种罕见的淋巴造血肿瘤,临床常以皮肤病变或淋巴结肿大为首发症状,临床过程具高度侵袭性,通常伴有骨髓侵犯。该肿瘤需与具有母细胞形态的淋巴系肿瘤和白血病相鉴别,诊断需结合临床信息、HE形态及免疫组化结果综合判断。Objective To summarize the diagnostic experiences of blastic plasmacytoid dendritic cell neoplasm(BPDCN)based on the study of its clinicopathological features and immunophenotypes.Methods The clinical data of 2 patients with BPDCN were collected,the structure alteration and cell morphology were observed by HE staining,the immunophenotype of tumor cells were studied by immunohistochemistry staining and flow cytometry was adopted to confirm the bone marrow involvement.Results Two patients,one of whom was a 97 year-old female,presented with cutaneous ecchymosis nodules as the first symptom.The epidermis,but not the dermal,was diffusedly infiltrated by tumor cells,which were medium-sized with irregular nuclei without prominent nucleoli.The other case was a 69 year-old male with lymph node enlargement as the first symptom.The skin was normal,but the lymph nodes were invasively destroyed by tumor cells,which were medium-sized blast-like with prominent nucleoli.The immunophenotypes of the two patients were both positive for CD123,CD4,CD56 and TDT,but negative for B,T lymphocyte derived and myeloid origin markers,both of which involved bone marrow.Conclusions BPDCN is a rare form of hematological neoplasm,skin symptoms or lymph node enlargement may be presented as the initial symptom,the clinical course were highly aggressive with high frequency of bone marrow involvement.The blastic-like lymphoma and leukemia entities should be considered into account for differential diagnose.The precise diagnosis of BPDCN should be established by integrating histomorphology,immunophenotype and clinical presentation information comprehensively.

关 键 词：母细胞性浆细胞样树突细胞肿瘤 皮肤 淋巴结 免疫表型 

分 类 号：R733[医药卫生—肿瘤]