Do Ngan, Ringold Sarah, Brandling-Bennett Heather
University of Washington School of Medicine, Seattle, Washington.
Department of Pediatrics, Division of Rheumatology, University of Washington/Seattle Children's Hospital, Seattle, Washington.
Pediatr Dermatol. 2019 Nov;36(6):932-935. doi: 10.1111/pde.14005. Epub 2019 Oct 2.
Cutaneous polyarteritis nodosa (CPAN) is a rare necrotizing vasculitis affecting small- to medium-sized arteries. Reported treatments include oral corticosteroids alone or in combination with non-steroidal antiinflammatory drugs, intravenous immunoglobulins, cyclophosphamide, azathioprine, colchicine, or dapsone. However, some patients with CPAN do not respond to such treatments and continue to experience exacerbations over prolonged periods. This series provides support for the use of TNF-α inhibitors in the treatment of recalcitrant CPAN in pediatric patients.
皮肤型结节性多动脉炎(CPAN)是一种罕见的坏死性血管炎,累及中小动脉。报道的治疗方法包括单独使用口服糖皮质激素或与非甾体抗炎药联合使用、静脉注射免疫球蛋白、环磷酰胺、硫唑嘌呤、秋水仙碱或氨苯砜。然而,一些CPAN患者对这些治疗无反应,并且在较长时间内持续病情加重。本系列研究为使用肿瘤坏死因子-α抑制剂治疗小儿难治性CPAN提供了支持。