Hafezi-Bakhtiari Sara, Al-Habeeb Ayman, Ghazarian Danny
Pathology Department, University Health Network, Toronto General Hospital, Toronto, Canada.
J Cutan Pathol. 2010 Sep;37(9):e46-9. doi: 10.1111/j.1600-0560.2009.01329.x. Epub 2009 Jul 10.
A 71-year-old man presented with a slowly growing 2.0x2.0x1.0 cm scalp lesion that was surgically removed. Microscopic examination showed a well-circumscribed dermally located tumor composed of ductal elements lined by double to multiple cell layers of bland cuboidal inner cells and elongated spindled outer cells with areas showing cribriform and solid growth patterns. Some cells showed prominent cytoplasmic clearing. A few mitotic figures are noted ranging from 1-2 mitotic figure/10 hpf. There are also foci of squamous differentiation as well as occasional mature adipocytes. The background stroma was predominantly sclerotic with only small area of myxoid background (confirmed by Hale's colloidal iron). Immunohistochemical studies revealed positive immunoreactivity for EMA, CEA, CD117, HWMK, LWMK, CK7, Androgen receptor and S100 in the ductal (epithelial) cells and positive immunereactivity for calponin, SMA, CK 5/6 and p63 in the myoepithelial component. No immunoreactivity for Brst-2, ER, PR and CK20 was noted. MIB-1 showed mildly increased proliferrative index highlighting 5% of the nuclei. The overall morphology and immunohistochemical profile are that of a benign cutanoues mixed tumor (chondroid syringoma). Given the unusual striking celluarlity, we suggest to subclassify this as a hyper-cellular variant.
一名71岁男性患者头皮出现一个缓慢生长的2.0×2.0×1.0 cm病变,已手术切除。显微镜检查显示,肿瘤位于真皮,边界清晰,由导管成分组成,导管内衬有双层至多层温和的立方状内层细胞和细长的梭形外层细胞,部分区域呈筛状和实性生长模式。部分细胞可见明显的胞质透亮。每10个高倍视野可见1 - 2个有丝分裂象。还有鳞状分化灶以及偶尔的成熟脂肪细胞。背景基质主要为硬化性,仅有小面积黏液样背景(经黑尔胶体铁证实)。免疫组化研究显示,导管(上皮)细胞中EMA、CEA、CD117、高分子量角蛋白、低分子量角蛋白、CK7、雄激素受体和S100呈阳性免疫反应,肌上皮成分中钙调蛋白、平滑肌肌动蛋白、CK 5/6和p63呈阳性免疫反应。未发现Brst-2、雌激素受体、孕激素受体和CK20的免疫反应。MIB-1显示增殖指数轻度升高,5%的细胞核被标记。总体形态和免疫组化特征符合良性皮肤混合瘤(软骨样汗管瘤)。鉴于其显著的细胞增多现象不常见,我们建议将其归类为高细胞变异型。