Moioli Eduardo K, Hsieh Clifford, Tisch Angela, Bolotin Diana
Department of Dermatology, University of Pennsylvania, Philadelphia, Pennsylvania.
Section of Dermatology, University of Chicago, Chicago, Illinois.
Dermatol Surg. 2018 Mar;44(3):341-349. doi: 10.1097/DSS.0000000000001300.
The histologic status of squamous cell carcinoma in situ (SCC-IS) after diagnostic biopsy has not been well described or compared between immunocompetent and immunosuppressed patients. Expression of immunohistochemical (IHC) markers of aggressive SCC has not been compared between SCC-IS that clears or becomes invasive after biopsy.
To determine the histologic status of SCC-IS after diagnostic biopsy in these populations.
Retrospective analysis of 129 patients with SCC-IS treated with excision and 55 patients treated with Mohs surgery. Histologic features of SCC in excised tissue after biopsy were recorded. Known SCC markers were evaluated using IHC.
Invasive SCC was found in 3% to 16% of residual SCC-IS depending on surgical treatment modality. The history of skin cancer increased the odds of having invasive SCC in SCC-IS excisions (odds ratio 7.1, p < .05). Forty-seven percent of SCC-IS in immunosuppressed patients cleared after diagnostic biopsy compared with 70% in immunocompetent patients (p < .05). Inflammatory infiltrate and molecular markers of aggressive SCCs (Ki-67, matrix metalloproteinase [MMP]-9, MMP-7, transforming growth factor-beta (TGFβ)-RI, TGFβ-RII, and Sox-2) were not predictive of residual or invasive SCC at the time of treatment.
Up to 16% of SCC-IS showed invasive SCC at the time of surgical treatment. Immunosuppressed patients are more likely to have residual disease after biopsy. IHC markers of invasive SCC may not predict invasion.
在免疫功能正常和免疫抑制的患者中,诊断性活检后原位鳞状细胞癌(SCC-IS)的组织学状态尚未得到充分描述或比较。活检后清除或发生侵袭的SCC-IS之间,侵袭性SCC的免疫组化(IHC)标志物表达尚未进行比较。
确定这些人群中诊断性活检后SCC-IS的组织学状态。
对129例行切除治疗的SCC-IS患者和55例行Mohs手术治疗的患者进行回顾性分析。记录活检后切除组织中SCC的组织学特征。使用IHC评估已知的SCC标志物。
根据手术治疗方式,残余SCC-IS中3%至16%发现有侵袭性SCC。皮肤癌病史增加了SCC-IS切除术中发生侵袭性SCC的几率(优势比7.1,p <.05)。免疫抑制患者中47%的SCC-IS在诊断性活检后清除,而免疫功能正常患者中这一比例为70%(p <.05)。侵袭性SCC的炎症浸润和分子标志物(Ki-67、基质金属蛋白酶[MMP]-9、MMP-7、转化生长因子-β(TGFβ)-RI、TGFβ-RII和Sox-2)在治疗时不能预测残余或侵袭性SCC。
高达16%的SCC-IS在手术治疗时显示有侵袭性SCC。免疫抑制患者活检后更有可能有残留疾病。侵袭性SCC的IHC标志物可能无法预测侵袭情况。