Du Amy X, Gniadecki Robert, Storek Jan, Osman Mohamed
Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Division of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Front Med (Lausanne). 2022 Feb 24;9:855740. doi: 10.3389/fmed.2022.855740. eCollection 2022.
Systemic sclerosis, also known as scleroderma, is an autoimmune disease characterized by cutaneous and visceral fibrosis, immune dysregulation, and vasculopathy. Generally, the degree of skin fibrosis is associated with an increased likelihood of visceral organ involvement. Its pathogenesis is poorly understood; however, it is clear that changes in both the innate and adaptive immune responses are associated with fibroblast dysfunction and vascular damage. Further, DNA damage has been postulated as one of the triggering factors in systemic sclerosis, although the association of DNA damage with the progression of this disease is more poorly established. Recently, abnormal DNA damage response repair pathways have also been identified in patients with systemic sclerosis, suggesting that cells from patients with this disease may be more susceptible to DNA damaging agents. Chemotherapeutic drugs and other DNA damaging agents have been associated with the development of systemic sclerosis, as these agents may provide additional "hits" that promote abnormal DNA damage responses and subsequent inflammatory changes. Herein, we present the case of a 39-year-old female who developed scleroderma after the treatment of her breast cancer with chemotherapeutic agents. Her scleroderma was subsequently successfully treated with autologous hematopoietic stem cell transplantation. We also completed a literature review for previously published cases of chemotherapy associated with systemic sclerosis and highlighted a role of DNA damage in promoting the disease. Our case is the first case of chemotherapy associated with systemic sclerosis treated with hematopoietic stem cell transplantation.
系统性硬化症,也称为硬皮病,是一种自身免疫性疾病,其特征为皮肤和内脏纤维化、免疫失调以及血管病变。一般来说,皮肤纤维化的程度与内脏器官受累的可能性增加相关。其发病机制尚不清楚;然而,很明显先天性和适应性免疫反应的变化都与成纤维细胞功能障碍和血管损伤有关。此外,尽管DNA损伤与该疾病进展之间的关联更不明确,但DNA损伤已被假定为系统性硬化症的触发因素之一。最近,在系统性硬化症患者中也发现了异常的DNA损伤反应修复途径,这表明该疾病患者的细胞可能对DNA损伤剂更敏感。化疗药物和其他DNA损伤剂与系统性硬化症的发生有关,因为这些药物可能提供额外的“刺激”,促进异常的DNA损伤反应和随后的炎症变化。在此,我们报告一例39岁女性在接受化疗药物治疗乳腺癌后发生硬皮病的病例。她的硬皮病随后通过自体造血干细胞移植成功治愈。我们还对先前发表的与系统性硬化症相关的化疗病例进行了文献综述,并强调了DNA损伤在促进该疾病中的作用。我们的病例是首例接受造血干细胞移植治疗的与系统性硬化症相关的化疗病例。