Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
Mod Pathol. 2013 Oct;26(10):1382-9. doi: 10.1038/modpathol.2013.75. Epub 2013 Apr 19.
Basal cell carcinoma of the anal region is rare and morphologically difficult to distinguish from basaloid squamous cell carcinoma, particularly on biopsies. This distinction has therapeutic and prognostic implications. We reviewed morphological features of 9 basal cell carcinomas and 15 basaloid squamous cell carcinomas from the anal region diagnosed during 1993-2011 and determined the utility of Ber-EP4, BCL2, TP63, CK5/6, CDKN2A, and SOX2 as diagnostic tools. Immunostains were scored in a semi-quantitative manner (1+-1-10%, 2+-11-50%, 3+->50%). All basal cell carcinomas were located in the perianal region, while all basaloid squamous cell carcinomas originated in the anal canal/anorectum. Nodular subtype of basal cell carcinoma was the most common subtype. Retraction artifact was the only significant distinguishing histological feature of basal cell carcinoma compared with basaloid squamous cell carcinoma (88% vs 26%; P=0.04). Atypical mitoses were more common in basaloid squamous cell carcinomas (71% vs 11%; P=0.05). An in situ component was only present in basaloid squamous cell carcinomas, and was noted in 6/15 cases. Basal cell carcinomas had 2-3+ Ber-EP4 (basal cell carcinoma 100% vs basaloid squamous cell carcinoma 40%; P<0.001) and BCL2 immunoreactivity (basal cell carcinomas 100% vs basaloid squamous cell carcinoma 33%; P<0.001). Diffuse CDKN2A and SOX2 expression was seen only in basaloid squamous cell carcinomas (basal cell carcinoma 0% vs basaloid squamous cell carcinoma 93%; P<0.001). There was no difference in TP63 and CK5/6 expression. Perianal location, retraction artifact, and lack of atypical mitoses are histological features that help distinguish basal cell carcinoma from basaloid squamous cell carcinoma. An in situ component, when present, supports the diagnosis of basaloid squamous cell carcinoma. Immunostains are extremely helpful as diffuse Ber-EP4 and BCL2 expression is a feature of basal cell carcinoma and basaloid squamous cell carcinoma is typified by diffuse CDKN2A and SOX2 expression.
肛门区域的基底细胞癌罕见,形态学上难以与基底样鳞状细胞癌区分,尤其是在活检时。这种区分具有治疗和预后意义。我们回顾了 1993 年至 2011 年间诊断的 9 例肛门区域基底细胞癌和 15 例基底样鳞状细胞癌的形态学特征,并确定了 Ber-EP4、BCL2、TP63、CK5/6、CDKN2A 和 SOX2 作为诊断工具的效用。免疫染色以半定量方式评分(1+-1-10%、2+-11-50%、3+->50%)。所有基底细胞癌均位于肛周区域,而所有基底样鳞状细胞癌均起源于肛管/直肠。基底细胞癌最常见的亚型为结节型。与基底样鳞状细胞癌相比,退缩性假设有组织学特征(88%对 26%;P=0.04),这是基底细胞癌唯一显著的鉴别特征。不典型有丝分裂在基底样鳞状细胞癌中更为常见(71%对 11%;P=0.05)。原位成分仅见于基底样鳞状细胞癌,15 例中有 6 例存在原位成分。基底细胞癌有 2-3+的 Ber-EP4(基底细胞癌 100%对基底样鳞状细胞癌 40%;P<0.001)和 BCL2 免疫反应性(基底细胞癌 100%对基底样鳞状细胞癌 33%;P<0.001)。仅基底样鳞状细胞癌弥漫表达 CDKN2A 和 SOX2(基底细胞癌 0%对基底样鳞状细胞癌 93%;P<0.001)。TP63 和 CK5/6 的表达无差异。肛门位置、退缩性假设有组织学特征有助于区分基底细胞癌和基底样鳞状细胞癌,而无不典型有丝分裂则是基底细胞癌的特征。原位成分存在时,支持基底样鳞状细胞癌的诊断。免疫染色非常有帮助,因为弥漫性 Ber-EP4 和 BCL2 表达是基底细胞癌的特征,而基底样鳞状细胞癌的特征是弥漫性 CDKN2A 和 SOX2 表达。