非特异性大动脉炎(Takayasu病)

G. Isayeva, S. Trypilka
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引用次数: 1

摘要

本文报告一例高松病(非特异性大动脉炎)的临床病例。本文以一位年轻女性的病程为例,分析了其临床症状特点和诊断难点。特别注意的是血管病变的可视化和随着疾病进展血管变化的动态评估。实验室参数的变化将根据正在进行的治疗详细介绍。对药物治疗本病疗效的文献资料进行分析。需要强调的是,文献中有非常有限数量的高质量安慰剂对照研究。执业医师在决策过程中只能依靠观察性研究的结果。此外,文献中所有的研究都包含了非常少的患者。给出了以糖皮质激素为第一行的治疗处方算法。虽然文献资料很少,但值得注意的是,在50%的患者中观察到孤立糖皮质激素治疗的缓解效果。根据最新的EULAR建议,在疾病确诊后,应立即开始治疗,推荐的起始剂量为40 - 60mg强的松龙(或同等剂量)。在病情得到控制后,建议1年后2 ~ 3个月逐渐减少剂量至目标15 ~ 20mg /天至10mg /天。下一步是开一种非糖皮质激素免疫抑制剂,以提供“类固醇节约”效果和长期控制疾病。所有关于甲氨蝶呤、霉酚酸酯、环磷酰胺、来氟酰胺和硫唑嘌呤疗效的现有信息都来自开放标签前瞻性或回顾性研究,参与者数量有限。肿瘤坏死因子抑制剂和托珠单抗被推荐为二线药物。在接受托珠单抗治疗的患者中,超过80%的患者有满意的临床和实验室反应。在这个临床病例中,使用了tocilizumab,并详细描述了该药在治疗8个月期间的效果。tocilizumab的免疫生物学治疗与良好的临床和实验室反应,血管狭窄的减少和患者健康的改善有关。
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Nonspecific aortoarteritis (Takayasu’s disease)
The article presents a clinical case of Takayasu’s disease (nonspecific aortoarteritis). On the example of the course of the disease in a young woman, the features of clinical symptoms and diagnostic difficulties are analyzed. Particular attention is paid to the visualization of vascular lesions and the assessment of the dynamics of changes in the vessels as the disease progresses. Changes in laboratory parameters are presented in details according with ongoing therapy. The analysis of literature data of the effectiveness of drug therapy for the disease was carried out. It is emphasized that there is a very limited number of quality placebo-controlled studies in the literature. The practicing physician can only rely on the results of observational studies in his decision’s making process. Also, all studies presented in the literature included a very small number of patients. The algorithm of therapy prescription is given, the first line of which is glucocorticoids. Although there are very few literature data, it is noted that the achievement of remission with isolated glucocorticoid therapy is observed in 50 % of patients. According to the updated EULAR recommendations, after disease verification, therapy should be initiated immediately, the recommended starting dose is 40–60 mg of prednisolone (or equivalent). After achieving control of the disease, it is recommended to gradually reduce the dose to the target 15–20 mg/day for 2 to 3 months after 1 year to 10 mg/day. The next step is to prescribe a non-glucocorticoid immunosuppressant in order to provide both a «steroid sparing» effect and long-term control under the disease. All available information on the efficacy of methotrexate, mycophenolate mofetil, cyclophosphophomide, leflunamide, and azathioprine comes from open-label prospective or retrospective studies with a limited number of participants. Tumor necrosis factor inhibitors and tocilizumab are recommended as second-line drugs. A satisfactory clinical and laboratory response was observed in more than 80 % of patients receiving tocilizumab therapy. In this clinical case, tocilizumab was used and the effects of the drug during treatment for 8 months are described in detail. Immunobiological therapy with tocilizumab was associated with a good clinical and laboratory response, a decrease in vascular stenosis, and an improvement in the patient’s well-being.
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