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首页> 外文期刊>Lupus >Successful rituximab therapy in a lupus patient with diffuse alveolar haemorrhage.
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Successful rituximab therapy in a lupus patient with diffuse alveolar haemorrhage.

机译:成功的利妥昔单抗疗法治疗弥漫性肺泡出血的狼疮患者。

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摘要

Diffuse alveolar haemorrhage (DAH) is a rare but life-threatening complication of systemic lupus erythematosus (SLE). Specific therapy is based on a heavy immunosuppressive treatment that usually associates corticosteroid and cyclophosphamide boluses and plasma exchange. Despite this treatment, an early mortality rate of 20-50% is reported in the literature. Immunosuppression-related complications are responsible for further mortality and morbidity. Rituximab, a specific anti-CD20 antigen B-cell antibody, has been used with success for the treatment of several refractory autoimmune disorders, but rarely for SLE-induced DAH. We report here the first case of SLE-induced DAH treated successfully with rituximab without cyclophosphamide administration in a patient intolerant to cyclophosphamide. We review the two other cases of SLE-induced DAH managed with rituximab as a part of the immunosuppressive regimen.
机译:弥漫性肺泡出血(DAH)是系统性红斑狼疮(SLE)的一种罕见但危及生命的并发症。特异性疗法是基于重度免疫抑制疗法,通常将皮质类固醇和环磷酰胺推注与血浆置换联系起来。尽管进行了这种治疗,文献中报道了20-50%的早期死亡率。与免疫抑制有关的并发症是导致进一步的死亡率和发病率的原因。利妥昔单抗是一种特异性的抗CD20抗原B细胞抗体,已成功用于治疗多种难治性自身免疫性疾病,但很少用于SLE诱导的DAH。我们在这里报告了第一例SLE诱导的DAH,在不耐受环磷酰胺的患者中成功用利妥昔单抗治疗而未给予环磷酰胺。我们回顾了利妥昔单抗作为免疫抑制方案一部分治疗的SLE诱导DAH的其他两个案例。

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