Martora Fabrizio, Tommasino Nello, Battista Teresa, Potestio Luca, Megna Matteo
Section of Dermatology - Department of Clinical Medicine and Surgery, University of Naples Federico II, Napoli, Italy.
Clin Cosmet Investig Dermatol. 2025 Mar 18;18:617-626. doi: 10.2147/CCID.S512373. eCollection 2025.
This systematic review explores the increased cancer risk in patients with hidradenitis suppurativa (HS), particularly cutaneous squamous cell carcinoma (SCC) and lymphoma. Chronic inflammation and immune dysregulation in HS are identified as key factors contributing to malignant transformation, often observed in areas of prolonged tissue damage.
The NOTCH signaling pathway, disrupted by smoking, plays a dual role in cancer, acting as both a tumor suppressor and a proto-oncogene depending on the context. Mutations in NOTCH and TP53 are common in SCC linked to HS, with a prevalence of 0.5% to 4.6%, predominantly in men and localized to the buttock and anogenital regions. Histological analyses suggest that malignant transformation occurs within keratinized epithelium, supported by altered cytokeratin expression. Immune dysregulation in HS-affected areas, compounded by scarring and lymphatic disruption, further exacerbates tumorigenic potential. While anti-TNF-alpha therapies have been implicated in cancer risk, conflicting evidence and meta-analyses suggest no consistent increase in non-melanoma skin cancers (NMSC). Similarly, IL-17 inhibitors show potential risks but lack robust evidence in HS-specific populations.
In conclusion, HS-associated malignancies, particularly SCC, underscore the need for further research to elucidate the mechanisms linking chronic inflammation to cancer development. Insights from such studies could guide preventative and therapeutic strategies, improving outcomes for HS patients.
本系统评价探讨了化脓性汗腺炎(HS)患者患癌风险的增加,尤其是皮肤鳞状细胞癌(SCC)和淋巴瘤。HS中的慢性炎症和免疫失调被确定为促成恶性转化的关键因素,这在长期组织损伤区域经常可见。
因吸烟而破坏的NOTCH信号通路在癌症中起双重作用,根据具体情况既作为肿瘤抑制因子又作为原癌基因。NOTCH和TP53的突变在与HS相关的SCC中很常见,患病率为0.5%至4.6%,主要发生在男性中,且局限于臀部和肛门生殖器区域。组织学分析表明,恶性转化发生在角化上皮内,细胞角蛋白表达的改变支持了这一点。HS受累区域的免疫失调,再加上瘢痕形成和淋巴系统破坏,进一步加剧了致瘤潜力。虽然抗TNF-α疗法与癌症风险有关,但相互矛盾的证据和荟萃分析表明,非黑色素瘤皮肤癌(NMSC)并没有持续增加。同样,IL-17抑制剂显示出潜在风险,但在HS特定人群中缺乏有力证据。
总之,HS相关的恶性肿瘤,尤其是SCC,凸显了进一步研究以阐明慢性炎症与癌症发展之间联系机制的必要性。此类研究的见解可为预防和治疗策略提供指导,改善HS患者的预后。