Research Unit of Dermatopathology, Department of Dermatology, Medical University of Graz, Graz, Austria.
Am J Surg Pathol. 2010 Jan;34(1):75-87. doi: 10.1097/PAS.0b013e3181c5e26b.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a neoplasm derived from precursors of plasmacytoid dendritic cells. Cutaneous involvement represents often the first manifestation of the disease. We studied 45 skin biopsies from 33 patients (M:F=7.25:1; median age: 71 y; age range: 30 to 89) with BPDCN to delineate histopathologic and immunophenotypic features of this disease. Patients presented with generalized (n=18), localized (n=6), or solitary (n=9) macules, plaques, and/or tumors. Staging investigations at presentation were negative in 20 patients. Unusual histologic features included a perivascular/periadnexal pattern (6 biopsies from 4 patients) and the presence of pleomorphism of neoplastic cells with blastoid cells admixed with elongated, twisted, or hyperchromatic cells (observed in 24 specimens). Negativity of 1 among the 4 markers CD4, CD56, CD123, and TCL-1 was seen in 11 biopsies, and of 2 markers in 4 biopsies. Staining for CD68 revealed positivity of the majority of cells in 1 and of scattered cells in 24/37 stained cases. Terminal deoxynucleotidyl transferase was observed in 22/37 stained cases. Staining for Bcl-6, MUM-1 and FOX-P1 revealed positivity of a variable proportion of neoplastic cells in 16/30, 19/29, and 21/23 cases, respectively. Our study shows that cutaneous lesions of BPDCN display a greater variability of morphologic and phenotypic features than recognized earlier. Discrete perivascular infiltrates, pleomorphic morphology of neoplastic cells, and unusual phenotypic profiles may be the source of diagnostic pitfalls. These atypical variants should be recognized to make an early diagnosis and to manage properly patients with this aggressive hematological disorder.
原始滤泡树突状细胞肿瘤(BPDCN)是一种来源于浆细胞样树突状细胞前体的肿瘤。皮肤受累通常是该病的首发表现。我们研究了 33 例 BPDCN 患者的 45 份皮肤活检,以描绘该病的组织病理学和免疫表型特征。患者表现为全身性(n=18)、局限性(n=6)或孤立性(n=9)斑、斑块和/或肿瘤。20 例患者在就诊时的分期检查均为阴性。不典型的组织学特征包括血管周围/腺周模式(4 例患者的 6 份活检)和肿瘤细胞的多形性,其中可见母细胞样细胞与拉长、扭曲或深染细胞混合(24 例标本中观察到)。4 种标志物 CD4、CD56、CD123 和 TCL-1 中有 1 种标志物阴性的见于 11 份活检,2 种标志物阴性的见于 4 份活检。CD68 染色显示大多数细胞阳性(1 例)和 24/37 例染色的散在细胞阳性。22/37 例染色的病例中观察到末端脱氧核苷酸转移酶阳性。Bcl-6、MUM-1 和 FOX-P1 的染色显示,16/30、19/29 和 21/23 例患者的肿瘤细胞阳性比例不同。我们的研究表明,BPDCN 的皮肤病变表现出比以前认识到的更大的形态和表型特征的变异性。离散的血管周围浸润、肿瘤细胞的多形性形态和不寻常的表型特征可能是诊断陷阱的来源。这些不典型的变异应该被识别出来,以便早期诊断并对这种侵袭性血液疾病进行适当的治疗。