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肿瘤芽殖是一个客观的高危因素,与<4cm 的皮肤鳞状细胞癌转移和不良临床预后相关。

Tumor Budding Is an Objective High-risk Factor Associated With Metastasis and Poor Clinical Prognosis in Cutaneous Squamous Cell Carcinoma Sized <4 cm.

机构信息

Departments of Diagnostic Pathology.

Dermatology.

出版信息

Am J Surg Pathol. 2019 Jul;43(7):975-983. doi: 10.1097/PAS.0000000000001284.

Abstract

Although most cases of early cutaneous squamous cell carcinoma (CSCC) are indolent, a small subset metastasize and can be fatal. However, high-risk features of CSCC are controversial, and it is difficult to predict the biological behavior. In this study, we have tested the prognostic significance of tumor budding in CSCCs <4 cm in diameter. Hematoxylin and eosin-stained sections of surgically resected CSCCs (24 metastasizing and 24 nonmetastasizing cases) <4 cm in size were reviewed retrospectively. Tumor bud, defined as an isolated cancer cell or a cluster comprising<5 cells, was counted at a hot spot (1.23 mm), and graded between 1 and 3; grade 1: 0 to 4 buds; grade 2: 5 to 9 buds; and grade 3: ≥10 buds. Cases with grades 2 or 3 were regarded as positive for tumor budding. We found that tumor budding was positive in 83.3% of metastasizing CSCC, and 37.5% of nonmetastasizing CSCC (P<0.01). Moreover, CSCCs with grade 3 tumor budding showed worse disease-specific survival (P<0.01). Regarding interobserver reproducibility, the median κ value for tumor budding was significantly higher than that for histologic differentiation (P<0.01). In conclusion, tumor budding may be a valuable histologic marker for risk stratification of early CSCC in routine practice. Patients with tumor budding positive CSCC may benefit from evaluation and close follow-up for regional node metastasis.

摘要

虽然大多数早期皮肤鳞状细胞癌(CSCC)病例呈惰性,但一小部分会转移并可能致命。然而,CSCC 的高风险特征存在争议,且难以预测其生物学行为。在本研究中,我们检测了直径<4cm 的 CSCC 中肿瘤芽的预后意义。回顾性分析了手术切除的 CSCC(24 例转移和 24 例非转移病例)的苏木精和伊红染色切片。肿瘤芽定义为孤立的癌细胞或包含<5 个细胞的簇,在热点(1.23mm)处计数,并分为 1-3 级;1 级:0-4 个芽;2 级:5-9 个芽;3 级:≥10 个芽。2 级或 3 级病例被认为肿瘤芽阳性。我们发现,转移 CSCC 中 83.3%的肿瘤芽阳性,而非转移 CSCC 中为 37.5%(P<0.01)。此外,具有 3 级肿瘤芽的 CSCC 显示出更差的疾病特异性生存(P<0.01)。关于观察者间的可重复性,肿瘤芽的中位κ 值明显高于组织学分化(P<0.01)。总之,肿瘤芽可能是 CSCC 早期危险分层的一个有价值的组织学标志物。肿瘤芽阳性的 CSCC 患者可能受益于区域淋巴结转移的评估和密切随访。

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