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利妥昔单抗成功诱导治疗小儿孤立性少免疫性肺毛细血管炎致弥漫性肺泡出血

Successful Induction Treatment With Rituximab of Isolated Pauci-Immune Pulmonary Capillaritis Presenting as Diffuse Alveolar Hemorrhage in a Pediatric Patient.

机构信息

Divisions of Pediatric Pulmonology and Sleep Medicine, Children's Hospital Los Angeles, University of Southern California School of Medicine, Los Angeles, CA.

Department of Pediatric Rheumatology, Children's Hospital Los Angeles, University of Southern California School of Medicine, Los Angeles, CA.

出版信息

Chest. 2020 Nov;158(5):e225-e227. doi: 10.1016/j.chest.2020.06.022.

Abstract

Diffuse alveolar hemorrhage often presents as dyspnea, cough, or hemoptysis, and it is mediated by both immune and nonimmune processes. Isolated pauci-immune capillaritis (IPPC) is a rare diagnosis in which capillaritis, small-vessel vasculitis of the lung, is found on biopsy in the absence of an underlying systemic disorder. Traditionally, IPPC has been treated similarly to anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis with cyclophosphamide and glucocorticoids. However, few cases describing management options are available in the literature, especially among pediatric patients. Our report of successful induction of remission in an adolescent girl suggests that the combination of IV rituximab and pulse methylprednisolone may be a viable option for disease control in pediatric patients with IPPC.

摘要

弥漫性肺泡出血常表现为呼吸困难、咳嗽或咯血,其由免疫和非免疫过程介导。孤立性少免疫性毛细血管炎(IPPC)是一种罕见的诊断,其特征是在无潜在系统性疾病的情况下,活检发现毛细血管炎,即肺小血管血管炎。传统上,IPPC 的治疗方法与抗中性粒细胞胞质自身抗体(ANCA)相关性血管炎相似,采用环磷酰胺和糖皮质激素。然而,文献中很少有描述治疗选择的病例,尤其是在儿科患者中。我们报告了一名青少年女性成功诱导缓解的病例,提示 IV 利妥昔单抗联合脉冲甲基强的松龙可能是治疗儿科 IPPC 患者疾病的一种可行选择。

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