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波生坦与西地那非联合治疗一名30岁系统性硬化症女性难治性指端溃疡和雷诺现象:病例报告及文献综述

Combination therapy with bosentan and sildenafil for refractory digital ulcers and Raynaud's phenomenon in a 30-year-old woman with systemic sclerosis: Case report and literature review.

作者信息

Rademacher Jan-Gerd, Wincup Chris, Tampe Björn, Korsten Peter

机构信息

Department of Nephrology and Rheumatology, University Medical Center Göttingen, Göttingen, Germany.

Department of Rheumatology, University College London, London, UK.

出版信息

J Scleroderma Relat Disord. 2020 Jun;5(2):159-164. doi: 10.1177/2397198319876738. Epub 2019 Sep 19.

Abstract

BACKGROUND

Systemic sclerosis is a rare autoimmune disease characterized by skin and organ fibrosis, and vasculopathy. Raynaud's phenomenon is almost universally present in systemic sclerosis and can be the most debilitating symptom. Raynaud's phenomenon may lead to the development of digital ulcers, potentially complicated by infection, tissue necrosis, and auto-amputation. Recommended treatments have variable efficacy.

METHODS

We report the case of a 30-year-old woman with diffuse systemic sclerosis suffering from severe Raynaud's phenomenon and digital ulcers with digital tissue necrosis who was treated with combination therapy of an endothelin receptor antagonist and phosphodiesterase 5 inhibitor. In addition, we reviewed the literature on the topic.

RESULTS

Previous therapy with calcium-channel blockers, intravenous iloprost, and bosentan had all failed to control symptoms. We added sildenafil in combination with bosentan and observed a rapid and sustained treatment effect. Raynaud's phenomenon severity, number of attacks, and attack duration decreased within 2 weeks of initiating treatment. Furthermore, this resulted in the healing of established digital ulcers.

CONCLUSION

Our case report suggests that combination therapy may be a feasible treatment for the most severely affected and refractory patients. In our literature review, we found one retrospective study and three additional cases with similarly encouraging results.

摘要

背景

系统性硬化症是一种罕见的自身免疫性疾病,其特征为皮肤和器官纤维化以及血管病变。雷诺现象在系统性硬化症中几乎普遍存在,且可能是最使人衰弱的症状。雷诺现象可能导致指端溃疡的发生,可能并发感染、组织坏死和自行截肢。推荐的治疗方法疗效各异。

方法

我们报告了一例30岁弥漫性系统性硬化症女性患者的病例,该患者患有严重的雷诺现象和伴有指端组织坏死的指端溃疡,接受了内皮素受体拮抗剂和磷酸二酯酶5抑制剂的联合治疗。此外,我们回顾了关于该主题的文献。

结果

先前使用钙通道阻滞剂、静脉注射伊洛前列素和波生坦治疗均未能控制症状。我们加用西地那非与波生坦联合治疗,并观察到快速且持续的治疗效果。在开始治疗的2周内,雷诺现象的严重程度、发作次数和发作持续时间均有所下降。此外,这使得已有的指端溃疡愈合。

结论

我们的病例报告表明,联合治疗可能是对受影响最严重且难治的患者的一种可行治疗方法。在我们的文献回顾中,我们发现一项回顾性研究和另外三例病例也有类似令人鼓舞的结果。

相似文献

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Rheopheresis for Digital Ulcers and Raynaud's Phenomenon in Systemic Sclerosis Refractory to Conventional Treatments.
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Rheumatology (Oxford). 2006 Oct;45 Suppl 3:iii45-8. doi: 10.1093/rheumatology/kel290.

引用本文的文献

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Raynaud's Phenomenon: A Current Update on Pathogenesis, Diagnostic Workup, and Treatment.
Vasc Specialist Int. 2024 Jul 23;40:26. doi: 10.5758/vsi.240047.
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Exploring the Multifaceted Potential of Sildenafil in Medicine.
Medicina (Kaunas). 2023 Dec 17;59(12):2190. doi: 10.3390/medicina59122190.

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