首页> 外文期刊>srpski arhiv za celokupno lekarstvo >Squamous cell skin carcinoma due to chronic sacrococcygeal diseases
【24h】

Squamous cell skin carcinoma due to chronic sacrococcygeal diseases

机译:慢性骶尾部疾病引起的鳞状细胞皮肤癌

获取原文
获取原文并翻译 | 示例

摘要

Introduction/Objective Sacrococcygeal region squamous cell cancers (SCC) due to chronic sacrococcygeal diseases of skin are rare malignancies. The anatomical relation with the anus represents a challenge for diagnosis and surgical treatment. The oncological treatment algorithm is still controversial. Here, we investigated the clinicopathologic features of skin cancer of the sacrococcygeal region in a total of 10 cases from a surgical oncology reference center. Methods We retrospectively analyzed the patients who underwent surgery for sacrococcygeal region skin SCC between January 2010 and July 2020. Results All patients were male, and the mean age was 52.9 +/- 10.5 years. In the etiology, five patients had hidradenitis suppurativa, two had human papillomavirus-associated condyloma (Buschke-Lowenstein tumor), and three had pilonidal sinus disease. The mean time between the development of the lesion and malignancy diagnosis was 21.7 +/- 5.8 years. In the preoperative evaluation, three patients had bone invasion. None of the patients had anal sphincter or rectal invasion. Also, no patient had lymph node metastasis or distant metastasis. Wide local excision (WLE) was performed in all patients, with three of them with bone resection. Adjuvant chemoradiotherapy was applied to five patients. In 28.5 +/- 13.7 months follow-up, local recurrence occurred in five patients and WLE was performed again in these patients. Of these five patients, two eventually became metastatic. Finally, three patients died due to the disease and six patients are still disease free. Conclusion Sacrococcygeal region SCCs may rarely develop after a long interval from hidradenitis suppurativa, pilonidal sinus disease, and condyloma acuminata. Anal sphincter-sparing WLE can be applied, but sphincter dysfunction may occur. The disease is associated with a high risk of relapse and poor survival.
机译:简介/目的 骶尾部慢性皮肤部疾病引起的骶尾部鳞状细胞癌(SCC)是一种罕见的恶性肿瘤。与肛门的解剖学关系对诊断和手术治疗提出了挑战。肿瘤治疗算法仍存在争议。在这里,我们调查了来自外科肿瘤学参考中心的总共 10 例骶尾部区域皮肤癌的临床病理特征。方法 回顾性分析2010年1月至2020年7月行骶尾部皮肤鳞状细胞癌手术的患者。结果 所有患者均为男性,平均年龄为52.9+/- 10.5岁。在病因学方面,5例患者为化脓性汗腺炎,2例患者为人瘤病毒相关性尖锐湿疣(Buschke-Lowenstein肿瘤),3例患者为藏毛窦疾病。病变发展和恶性肿瘤诊断之间的平均时间为 21.7 +/- 5.8 年。术前评估发现3例患者出现骨浸润。所有患者均无肛门括约肌或直肠浸润。此外,没有患者有淋巴结转移或远处转移。所有患者均行宽局部切除术(WLE),其中3例行骨切除术。对5例患者进行了辅助放化疗。在 28.5 +/- 13.7 个月的随访中,5 例患者发生局部复发,并再次对这些患者进行 WLE。在这 5 名患者中,有 2 名最终发生转移。最后,三名患者因该疾病死亡,六名患者仍未患病。结论 骶尾部鳞状细胞癌在化脓性汗腺炎、藏毛窦病和尖锐湿疣后间隔较长后很少发生。可以应用保留肛门括约肌的 WLE,但可能会发生括约肌功能障碍。该疾病与复发风险高和生存率低有关。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号