Wang Lora S, Handorf Elizabeth A, Wu Hong, Liu Jeffrey C, Perlis Clifford S, Galloway Thomas J
Departments of *Radiation Oncology †Biostatistics ‡Pathology ∥Dermatology, Fox Chase Cancer Center §Department of Surgical Oncology, Head and Neck Surgery Section, Temple University Hospitals, Philadelphia, PA.
Am J Clin Oncol. 2017 Aug;40(4):429-432. doi: 10.1097/COC.0000000000000178.
Skin adnexal carcinoma (SAC) is a rare cutaneous malignancy that arises from sebaceous and sweat glands. These carcinomas are believed to behave more aggressively than cutaneous squamous cell carcinomas (SCC) with a propensity for local recurrence. The role of adjuvant radiotherapy in SAC is undefined.
We retrospectively reviewed all cases of head and neck SAC treated with surgery and adjuvant radiation from 2000 to 2012 at a single institution.
Nine cases were identified. Median age was 67 (range, 52 to 88) years. The histologies were: adnexal carcinoma (n=1), adnexal carcinoma with sebaceous differentiation (n=1), adnexal carcinoma with squamous differentiation (n=1), skin appendage carcinoma (n=1), sclerosing sweat duct carcinoma (n=1), mucinous carcinoma (n=1), ductal eccrine adenocarcinoma (n=1), porocarcinoma (n=1), and trichilemmal carcinoma (n=1). All tumors were reviewed by a dermatopathologist to confirm the SAC diagnosis.All patients had undergone surgery. Indications for adjuvant radiation included involved lymph nodes (n=4), perineural invasion (n=2), nodal extracapsular extension (n=2), positive margin (n=1), high-grade histology (n=6), multifocal disease (n=2), and/or recurrent disease (n=5). Radiation was delivered to the primary site alone (n=3), to the draining lymphatics alone (n=2), or to both (n=4). One patient received concurrent cisplatin. Median dose to the primary site was 60 Gy and to the neck was 50 Gy.Median follow-up was 4.0 years (range, 0.6 to 11.4 y). Locoregional control was 100%. Five-year progression-free survival was 89%. There was 1 acute grade 3 toxicity and no greater than or equal to grade 2 late toxicities were recorded.
Surgery and adjuvant radiation for high-risk SAC offers excellent locoregional control with acceptable toxicity.
皮肤附属器癌(SAC)是一种罕见的皮肤恶性肿瘤,起源于皮脂腺和汗腺。据信这些癌比皮肤鳞状细胞癌(SCC)侵袭性更强,且有局部复发倾向。辅助放疗在SAC中的作用尚不明确。
我们回顾性分析了2000年至2012年在单一机构接受手术及辅助放疗的所有头颈部SAC病例。
共识别出9例。中位年龄为67岁(范围52至88岁)。组织学类型包括:附属器癌(n = 1)、皮脂腺分化的附属器癌(n = 1)、鳞状分化的附属器癌(n = 1)、皮肤附属器癌(n = 1)、硬化性汗腺导管癌(n = 1)、黏液癌(n = 1)、导管小汗腺腺癌(n = 1)、汗孔癌(n = 1)和外毛根鞘癌(n = 1)。所有肿瘤均经皮肤病理学家复查以确诊SAC诊断。所有患者均接受了手术。辅助放疗的指征包括淋巴结受累(n = 4)、神经周围侵犯(n = 2)、淋巴结包膜外扩展(n = 2)、切缘阳性(n = 1)、高级别组织学(n = 6)、多灶性病变(n = 2)和/或复发性疾病(n = 5)。放疗仅针对原发部位(n = 3)、仅针对引流淋巴管(n = 2)或两者都进行(n = 4)。1例患者接受了顺铂同步治疗。原发部位的中位剂量为60 Gy,颈部为50 Gy。中位随访时间为4.0年(范围0.6至11.4年)。局部区域控制率为100%。5年无进展生存率为89%。有1例3级急性毒性反应,未记录到大于或等于2级的晚期毒性反应。
手术及辅助放疗用于高危SAC可提供良好的局部区域控制,且毒性可接受。