Roy Simon F, Lafaille Philippe, Désy Delphine
1 University of Montreal, Montreal, Quebec, Canada.
Int J Surg Pathol. 2019 Aug;27(5):518-520. doi: 10.1177/1066896919830208. Epub 2019 Feb 14.
We report the case of a 94-year-old man with a rapidly growing nodule on the preauricular area, which on histology showed a poorly differentiated spindle cell tumor with negative p63 and p40 antibody immunostains, negative high- and low-molecular-weight cytokeratins albeit for a focal expression of cytokeratin AE1/AE3. Spindle cell melanoma, angiosarcoma, and leiomyosarcoma were excluded. We explore the diagnostic approach to this challenging conundrum. Certain authors have suggested that sarcomatoid carcinoma and atypical fibroxanthoma (AFX) may lie within a spectrum of "sarcoma-like tumors of the head and neck" and that they may all run a similarly indolent clinical course. However, AFX appears to remain a diagnosis of exclusion, and expert consensus is that by definition AFX cannot express any cytokeratin antigens.
我们提供我们报告了一例94岁男性患者,其耳前区有一个快速生长的结节,组织学检查显示为低分化梭形细胞肿瘤,p63和p40抗体免疫染色阴性,高分子量和低分子量细胞角蛋白均为阴性,不过细胞角蛋白AE1/AE3有局灶性表达。排除了梭形细胞黑色素瘤、血管肉瘤和平滑肌肉瘤。我们探讨了针对这一具有挑战性难题的诊断方法。某些作者认为,肉瘤样癌和非典型纤维黄色瘤(AFX)可能属于“头颈部肉瘤样肿瘤”范畴,且它们可能都有相似的惰性临床病程。然而,AFX似乎仍是一种排除性诊断,专家共识是,根据定义,AFX不能表达任何细胞角蛋白抗原。