Breneman Alyssa, Bowling Anna, Trager Megan H, Gordon Emily R, Arron Sarah T, Samie Faramarz H
Department of Dermatology, Columbia University Irving Medical Center, 161 Ft Washington Ave, 12th Floor, New York, NY, 10032, USA.
Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
Arch Dermatol Res. 2025 Jan 6;317(1):172. doi: 10.1007/s00403-024-03710-w.
Sebaceous carcinoma is a rare cutaneous malignancy of sebaceous glands, but it is up to 25-fold more common in immunosuppressed individuals. In this narrative review, we examine the current literature on the pathogenesis, incidence, risk factors, prognosis, treatment, and surveillance of sebaceous carcinoma in immunosuppression and highlight practical considerations for providers who care for these patients. Increased incidence may be related to decreased immune surveillance, susceptibility to an unknown viral trigger, microsatellite instability, immunosuppressive medications, and unmasking of occult Muir-Torre Syndrome. Risk factors include type of immunosuppression, specific immunosuppressive medications and duration of treatment, and extensive solar damage. Prognosis may be similar to the general population, though data are conflicting. Treatment for primary sebaceous carcinoma is generally surgical, though in patients with high-risk tumors, adjuvant therapy may be advisable. Immunosuppressed patients should have regular screening skin exams, and those with a history of sebaceous carcinoma should have more frequent checks. Providers may consider genetic testing for patients with other features suggestive of occult Muir-Torre Syndrome. If found to have germline Muir-Torre Syndrome mutations, these patients require more rigorous surveillance.
皮脂腺癌是一种罕见的皮脂腺皮肤恶性肿瘤,但在免疫抑制个体中其发病率高达普通人群的25倍。在这篇叙述性综述中,我们研究了当前关于免疫抑制状态下皮脂腺癌的发病机制、发病率、危险因素、预后、治疗及监测的文献,并强调了为这些患者提供护理的医疗人员的实际注意事项。发病率增加可能与免疫监视功能下降、对未知病毒触发因素的易感性、微卫星不稳定性、免疫抑制药物以及隐匿性穆尔-托里综合征的暴露有关。危险因素包括免疫抑制类型、特定免疫抑制药物及治疗持续时间,以及广泛的日光损伤。预后可能与普通人群相似,尽管数据存在矛盾。原发性皮脂腺癌的治疗通常为手术治疗,不过对于高危肿瘤患者,辅助治疗可能是可取的。免疫抑制患者应定期进行皮肤筛查检查,有皮脂腺癌病史的患者应更频繁地检查。对于有其他提示隐匿性穆尔-托里综合征特征的患者,医疗人员可考虑进行基因检测。如果发现有生殖系穆尔-托里综合征突变,这些患者需要更严格的监测。