免疫抑制剂治疗系统性硬化症- ild伴曲霉菌瘤患者的单例体会

Wilujeng Anggraini, Perdana Rahman
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摘要

背景:系统性硬化症(SSc)是一种慢性自身免疫性疾病,对临床医生来说仍然是一个巨大的挑战。SSc的特征是免疫失调和进行性纤维化,通常会累及不同的内脏器官,如肺。间质性肺疾病(ILD)是SSc的常见表现,也是导致死亡的主要原因。免疫抑制药物是抑制SSc炎症过程的主要治疗方法。病例介绍:在这个病例中,我们报告了一个40岁的女性患有ILD-SSc。根据高分辨率计算机断层扫描(HRCT),我们发现这是间质性肺疾病伴曲菌瘤。她服用了甲基强的松龙3x8毫克和硫唑嘌呤2x50毫克。治疗结束时,患者临床情况有所改善,真菌曲菌瘤HRCT评价无恶化。结论:系统性硬化症(SSc)是一种罕见的自身免疫性疾病,累及皮肤和内脏器官。免疫抑制剂仍然是大多数自身免疫性疾病的首选药物。免疫抑制剂可能促进真菌生长,并与包括曲菌瘤在内的大多数严重真菌疾病的风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single Case Experience of Immunosuppressant Administration to Systemic Sclerosis-ILD Patients with Aspergilloma
Background: Systemic sclerosis (SSc) is a chronic autoimmune disease that still poses a great challenge to clinicians. SSc is characterized by immune dysregulation and progressive fibrosis that typically affects variable internal organ involvement such as lungs. Interstitial lung disease (ILD) is a common manifestation of SSc and a leading cause of death. The immunosuppressive drug is the main treatment to suppress the inflammation process in SSc. Case presentation: In this case we report a 40-year-old female to suffer ILD-SSc. According to High-Resolution Computed Tomography (HRCT) thorax, we found that it was interstitial lung disease with aspergilloma. She got methylprednisolone 3x8 mg and azathioprine 2x50 mg. At the end of the treatment, the patient showed improvement in her clinical condition and showed no worsening condition in the HRCT evaluation for her fungal aspergilloma. Conclusion: Systemic sclerosis (SSc) is a rare autoimmune disease involving the skin and internal organs. The immunosuppressive agent is still the drug of choice for most autoimmune diseases. Immunosuppressive may promote fungal growth and have been associated with increased risk in most serious fungal diseases including aspergilloma.
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