Kuwano H, Hashimoto H, Enjoji M
Cancer. 1985 Jan 1;55(1):172-80. doi: 10.1002/1097-0142(19850101)55:1<172::aid-cncr2820550127>3.0.co;2-f.
A clinicopathologic study was done of 21 cutaneous, sarcoma-like lesions previously diagnosed as atypical fibroxanthoma, spindle cell carcinoma, or dermal sarcoma. These lesions were most commonly presented as a solitary, often ulcerated nodule, occurring on exposed skin of the face in the elderly or, occasionally, on roentgen-damaged or burnt skin of the head, leg, or hand. Microscopic features of the 21 lesions were, however, not alike, thereby implying that such sarcoma-like lesions had derived from heterogeneous origins. The immunohistochemical staining in a comparative study with two other cases of unequivocal spindle cell squamous carcinoma suggested that these lesions could be histogenetically divided into two different groups: (1) the major group of true atypical fibroxanthoma, consisting of 19 cases, and (2) the minor group of probable spindle cell squamous carcinoma, consisting of 2 cases. Despite a wide histologic spectrum and of heterogeneity of these lesions, there was a benign clinical course in the majority, due in part to the small size and superficial location of the lesions.
对21例先前诊断为非典型纤维黄色瘤、梭形细胞癌或皮肤肉瘤的皮肤肉瘤样病变进行了临床病理研究。这些病变最常见的表现为单个、常伴有溃疡的结节,发生于老年人面部的暴露皮肤,或偶尔发生于头部、腿部或手部经X线照射损伤或烧伤的皮肤。然而,这21例病变的微观特征并不相同,这意味着此类肉瘤样病变起源各异。与另外两例明确的梭形细胞鳞状细胞癌进行对比研究的免疫组化染色结果表明,这些病变在组织发生学上可分为两个不同的组:(1)主要组为真正的非典型纤维黄色瘤,共19例;(2)次要组为可能的梭形细胞鳞状细胞癌,共2例。尽管这些病变的组织学谱广泛且具有异质性,但大多数病变临床病程呈良性,部分原因是病变体积小且位置表浅。