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生殖器基底细胞癌,其发病机制与暴露于阳光下的基底细胞癌不同?一项30例病例对照研究。

Genital basal cell carcinoma, a different pathogenesis from sun-exposed basal cell carcinoma? A case-control study of 30 cases.

作者信息

Wang Yen-Jen, Tang Tzu-Yin, Wang Jen-Yu, Huang Yen-Kai, Wu Yu-Hung

机构信息

Department of Dermatology, MacKay Memorial Hospital, Taipei, Taiwan.

Department of Pathology, MacKay Memorial Hospital, Taipei, Taiwan.

出版信息

J Cutan Pathol. 2018 Jun 19. doi: 10.1111/cup.13304.

Abstract

BACKGROUND

Genital basal cell carcinoma (BCC) accounts for <1% of all BCCs. We aimed to elucidate the pathogenesis of genital BCC.

METHODS

We retrospectively evaluated cases of pathologically diagnosed genital BCC between 1990 and 2016 in an Asian tertiary referral center. The control group was composed of consecutive cases, from 2016, of BCCs occurring in sun-exposed areas. Presence of human papillomavirus (HPV) was evaluated by polymerase chain reaction (PCR). Immunohistochemical p16 and p53 staining was performed and analyzed.

RESULTS

We found 33 genital BCCs (33/1837, 1.8%) over 26 years. The mean follow-up duration was 30.0 ± 33.2 months. Genital BCCs had a larger size (14.05 vs 8.92 mm, P = 0.014), more common presence of ulcers (61.3% vs 32.0%, P = 0.035), shorter epidermal p53 clone (0.33 vs 1.20 mm, P = 0.007), and high p53 expression levels. Most cases (29/30, 96.7%) showed negative or faint spotty p16 staining. Patient age, tumor depth, presence of pigment, or histology subtype did not differ significantly. Thirty genital BCCs were negative for HPV.

CONCLUSIONS

HPV infection is mostly likely not involved in genital BCC pathogenesis. A greater level of p53 expression in genital BCCs implicates pathways other than ultraviolet (UV)-specific p53 mutations in their pathogenesis.

摘要

背景

生殖器基底细胞癌(BCC)占所有基底细胞癌的比例不到1%。我们旨在阐明生殖器基底细胞癌的发病机制。

方法

我们回顾性评估了1990年至2016年在一家亚洲三级转诊中心经病理诊断的生殖器基底细胞癌病例。对照组由2016年以来在阳光暴露部位发生的基底细胞癌连续病例组成。通过聚合酶链反应(PCR)评估人乳头瘤病毒(HPV)的存在情况。进行免疫组织化学p16和p53染色并分析。

结果

在26年中我们发现了33例生殖器基底细胞癌(33/1837,1.8%)。平均随访时间为30.0±33.2个月。生殖器基底细胞癌的大小更大(14.05对8.92毫米,P = 0.014),溃疡更常见(61.3%对32.0%,P = 0.035),表皮p53克隆较短(0.33对1.20毫米,P = 0.007),且p53表达水平较高。大多数病例(29/30,96.7%)显示p16染色为阴性或弱阳性斑点状。患者年龄、肿瘤深度、色素沉着情况或组织学亚型无显著差异。30例生殖器基底细胞癌HPV检测为阴性。

结论

HPV感染很可能与生殖器基底细胞癌的发病机制无关。生殖器基底细胞癌中较高水平的p53表达表明其发病机制涉及紫外线(UV)特异性p53突变以外的其他途径。

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