Garcia J A, Cohen P R, Herzberg A J, Wallis M E, Rapini R P
Department of Dermatology, University of Texas-Houston Medical School 77030, USA.
J Am Acad Dermatol. 1995 May;32(5 Pt 1):740-6. doi: 10.1016/0190-9622(95)91452-8.
A variant of basal cell carcinoma (BCC) with scattered large, pleomorphic cells has previously been reported as "basal cell epithelioma with giant tumor cells" and "basal cell carcinoma with monster cells."
Our purpose was to describe the clinical, histologic, and DNA ploidy findings in BCCs with these cytologic features.
Nineteen pleomorphic BCCs from 15 patients were prospectively collected, and other BCCs in these patients were retrospectively reviewed by light microscopy. One lesion was recurrent. Seven of the pleomorphic BCCs and one nonpleomorphic BCC were studied by image analysis.
These pleomorphic BCCs ranged from 2.8 to 12.5 mm in greatest diameter and were most commonly located on the head and neck. Five BCCs were present on the face and scalp of a patient with basal cell nevus syndrome. There have been no subsequent recurrences of the pleomorphic BCCs (follow-up from 3 to 32 months; median, 20 months). All 19 pleomorphic BCCs displayed characteristic features of BCC: peripheral palisading, stromal retraction, mucin production, and apoptosis. All 19 also showed huge pleomorphic mononucleated and multinucleated giant tumor cells. The nuclei of these large cells were often hyperchromatic with prominent nucleoli and abundant cytoplasm, and occasionally with intranuclear cytoplasmic protrusions. In addition, there were frequent and atypical mitoses in 47% of the cases. All pleomorphic BCCs studied by cell image analysis of formalin-fixed, paraffin-embedded tissue were aneuploid. The DNA content of the giant tumor cells was not a multiple of a single DNA value.
Pleomorphic BCCs clinically present as typical BCCs. Despite their striking focal cellular atypia, these lesions seem to behave as ordinary BCCs.
先前曾报道过一种基底细胞癌(BCC)变体,其具有散在的大的多形性细胞,被称为“伴有巨细胞瘤细胞的基底细胞上皮瘤”和“伴有怪异细胞的基底细胞癌”。
我们的目的是描述具有这些细胞学特征的基底细胞癌的临床、组织学和DNA倍体结果。
前瞻性收集了15例患者的19个多形性基底细胞癌,并通过光学显微镜对这些患者的其他基底细胞癌进行回顾性分析。1例病变为复发性。对7个多形性基底细胞癌和1个非多形性基底细胞癌进行图像分析研究。
这些多形性基底细胞癌最大直径为2.8至12.5毫米,最常见于头颈部。1例基底细胞痣综合征患者的面部和头皮有5个基底细胞癌。多形性基底细胞癌无后续复发(随访3至32个月;中位数为20个月)。所有19个多形性基底细胞癌均表现出基底细胞癌的特征:外周栅栏状排列、间质退缩、黏液产生和凋亡。所有19个病例还显示有巨大的多形性单核和多核巨细胞瘤细胞。这些大细胞的细胞核常染色质增多,核仁突出,细胞质丰富,偶尔有核内细胞质突起。此外,47%的病例有频繁且不典型的有丝分裂。对福尔马林固定、石蜡包埋组织进行细胞图像分析研究的所有多形性基底细胞癌均为非整倍体。巨细胞瘤细胞的DNA含量不是单个DNA值的倍数。
多形性基底细胞癌临床上表现为典型的基底细胞癌。尽管有明显的局灶性细胞异型性,但这些病变的行为似乎与普通基底细胞癌相同。