Defty Clare L, Segen Joseph, Carter Jonathan J, Ahmed Imtiaz, Carr Richard A
Department of Dermatology, University Hospitals of Coventry & Warwickshire NHS Trust, Clifford Bridge Road, Coventry, UK.
J Cutan Pathol. 2011 Apr;38(4):354-6. doi: 10.1111/j.1600-0560.2010.01627.x. Epub 2010 Oct 5.
Pleomorphic giant or 'monster' cells represent a well-recognized yet uncommon finding associated with basal cell carcinoma (BCC), usually of nodular type. We present a case of basaloid squamous cell carcinoma (basaloid SCC) with 'monster' cells that closely mimicked those described in pleomorphic nodular BCC. Clinically, the lesion presented as a fleshy, hyperkeratotic nodule in an 82-year-old woman. Histopathology revealed a basaloid lesion with lobulated borders and focal retraction artifact but a lack of prominent palisading or stromal mucin. There were areas of necrosis and small foci of keratinization. Striking bizarre monstrous pleomorphic nuclei were widely scattered throughout the lesion. Ber-EP4 immunohistochemistry proved to be negative and epithelial membrane antigen (EMA) expression was moderate to strong in 70% of the basaloid epithelium. Monster cells have not previously been highlighted in cutaneous SCC or in its uncommon cutaneous basaloid variant. The prognostic significance of monster cells is unknown but, given the relative paucity of keratinization in basaloid SCC, these lesions should probably be regarded as poorly differentiated. We have not previously encountered an SCC that so closely resembles nodular BCC with pleomorphic monster cells and believe that this is the first such report in the literature.
多形性巨细胞或“怪物”细胞是与基底细胞癌(BCC)相关的一种公认但不常见的表现,通常为结节型。我们报告一例伴有“怪物”细胞的基底样鳞状细胞癌(基底样SCC),其与多形性结节型BCC中描述的细胞非常相似。临床上,该病变表现为一名82岁女性身上的肉质、角化过度结节。组织病理学显示为边界呈分叶状且有局灶性退缩假象的基底样病变,但缺乏明显的栅栏状排列或间质黏液。存在坏死区域和小灶性角化。显著怪异的多形性核广泛散在于整个病变中。Ber-EP4免疫组化结果为阴性,70%的基底样上皮中上皮膜抗原(EMA)呈中度至强阳性表达。此前,“怪物”细胞在皮肤SCC或其罕见的皮肤基底样变体中未被重点提及。“怪物”细胞的预后意义尚不清楚,但鉴于基底样SCC中角化相对较少,这些病变可能应被视为低分化。我们此前未曾遇到过如此酷似伴有多形性“怪物”细胞的结节型BCC的SCC,相信这是文献中首例此类报告。