Eatz Tiffany A, Elarjani Turki, Chen Stephanie H, Lu Victor M, Wu Eva M, Saad Ali G, Shah Ashish, Komotar Ricardo Jorge, Morcos Jacques J, Benjamin Carolina Gesteira, Ivan Michael E
Department of Neurological Surgery, University of Miami, Miller School of Medicine, Miami, Florida, USA.
Department of Neurological Surgery, University of Miami, Miller School of Medicine, Miami, Florida, USA.
World Neurosurg. 2023 Sep;177:e52-e65. doi: 10.1016/j.wneu.2023.05.039. Epub 2023 May 17.
We report a unique case of a suspected recurrent intracranial epidermoid cyst (EDC) that was found on pathology to have undergone malignant transformation to squamous cell carcinoma (SCC) approximately 25 years after initial resection. Additionally, we performed a systematic review including 94 studies reporting intracranial EDC to SCC transformation.
Ninety-four studies were included in our systematic review. PubMed, Scopus, Cochrane Central, and EMBASE were searched in April 2020 for studies regarding histologically confirmed SCC arising within an EDC. Kaplan-Meier estimations were used to estimate time to event including survival, and log rank tests were used to test for significance. All analyses were conducted using STATA 14.1 (StataCorp, College Station, Texas, USA); tests were two-sided, and statistical significance was defined using the alpha threshold of 0.05.
The overall median time to transformation was 60 months (95% confidence interval {CI}, 12-96). Transformation time was significantly shorter in the no surgery group (10 months, 95% CI undefined) versus the other 2 groups (60 months, 95% CI, 12-72 in surgery only and 70 months, 95% CI, 9-180 in surgery + adjuvant therapy group, both P < 0.01). Overall survival was significantly longer in the surgery + adjuvant therapy group (13 months, 95% CI, 9-24) versus the other 2 groups (3 months, 95% CI, 1-7 in surgery only and 6 months, 95% CI, 1-12 in the no surgery group, both P < 0.01).
We report a rare case of delayed malignant transformation of an intracranial EDC to SCC, occurring nearly 25 years after initial resection. Transformation time in the no-surgery group was statistically significantly shorter as compared to the surgery only and surgery + adjuvant therapy groups. Overall survival was statistically significantly higher in the surgery + adjuvant therapy group as compared to the surgery only and no surgery groups.
我们报告了一例罕见的疑似复发性颅内表皮样囊肿(EDC)病例,经病理检查发现其在初次切除后约25年发生了恶性转化为鳞状细胞癌(SCC)。此外,我们进行了一项系统综述,纳入了94项报告颅内EDC转化为SCC的研究。
我们的系统综述纳入了94项研究。2020年4月,在PubMed、Scopus、Cochrane Central和EMBASE数据库中检索关于组织学确诊的EDC内发生SCC的研究。采用Kaplan-Meier估计法估计包括生存时间在内的事件发生时间,并使用对数秩检验进行显著性检验。所有分析均使用STATA 14.1软件(美国德克萨斯州大学站的StataCorp公司)进行;检验为双侧检验,统计学显著性定义为α阈值为0.05。
转化的总体中位时间为60个月(95%置信区间{CI},12 - 96)。未手术组的转化时间(10个月,95% CI未定义)明显短于其他两组(单纯手术组为60个月,95% CI,12 - 72;手术 + 辅助治疗组为70个月,95% CI,9 - 180,两者P < 0.01)。手术 + 辅助治疗组的总生存期(13个月,95% CI,9 - 24)明显长于其他两组(单纯手术组为3个月,95% CI,1 - 7;未手术组为6个月,95% CI,1 - 12,两者P < 0.01)。
我们报告了一例罕见的颅内EDC延迟恶性转化为SCC的病例,发生在初次切除后近25年。与单纯手术组和手术 + 辅助治疗组相比,未手术组的转化时间在统计学上显著更短。与单纯手术组和未手术组相比,手术 + 辅助治疗组的总生存期在统计学上显著更高。