Suppr超能文献

儿童肉芽肿性多血管炎的坏疽性脓皮病样溃疡表现。

Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis.

机构信息

Section of Pediatric Rheumatology, University of Chicago Medical Center, Chicago, IL, USA.

Section of Dermatology, Department of Medicine, University of Chicago Medical Center, Chicago, IL, USA.

出版信息

Pediatr Rheumatol Online J. 2021 Jun 5;19(1):81. doi: 10.1186/s12969-021-00564-8.

Abstract

BACKGROUND

Granulomatosis with polyangiitis (GPA) is an anti-neutrophilic cytoplasmic antibody-associated vasculitis affecting small to medium-sized vessels and involves most commonly the kidneys and the respiratory tract. Skin involvement can be seen in up to 50% of children with GPA and is the initial presenting symptom in 7.7%. Pyoderma gangrenosum (PG)-like ulcers are rarely described as a skin manifestation in GPA and very few cases have been reported previously in children.

CASE PRESENTATION

We describe 3 new pediatric cases of GPA with PG-like ulcerations. The median age at first symptom was 15 years. Two patients had PG-like ulceration as their initial presentation; additional symptoms eventually led to the diagnosis of GPA 2-24 months later. In 1 case, proteinase 3 (PR3) was negative when first tested, but converted to positive when systemic symptoms emerged; in the other 2 cases PR3 was positive at presentation. All 3 patients had prominent facial lesions. None of the patients responded to treatment with antibiotics or medications commonly used to manage PG, including corticosteroids and cyclosporine. All patients had excellent responses to rituximab. An electronic database literature review was performed and 4 previously reported cases were identified. We assessed the clinical characteristics, serology, and response to treatment of the previously reported and our newly diagnosed cases.

CONCLUSION

PG-like ulceration is a rare presentation of pediatric GPA which may precede classic systemic GPA symptoms. The predominance of facial ulcer, granulomatous and neutrophilic inflammation on skin biopsy and lack of response to PG treatments are characteristic of GPA-associated PG-like ulcers. Our review suggests that treatment with rituximab may be needed to improve the skin lesions. Recognizing that PG-like ulcerations can occur in pediatric GPA may result in timely diagnosis, appropriate treatment and improved prognosis.

摘要

背景

肉芽肿性多血管炎(GPA)是一种抗中性粒细胞胞浆抗体相关性血管炎,影响小至中等大小的血管,最常累及肾脏和呼吸道。皮肤受累在多达 50%的 GPA 患儿中可见,是 GPA 的初始表现症状,占比 7.7%。坏疽性脓皮病(PG)样溃疡很少被描述为 GPA 的皮肤表现,以前在儿童中也很少有报道。

病例介绍

我们描述了 3 例新的 GPA 合并 PG 样溃疡的儿科病例。首次出现症状的中位年龄为 15 岁。2 例患者以 PG 样溃疡为首发表现;其他症状最终导致 GPA 的诊断,在 2-24 个月后确诊。1 例患者首次检测时蛋白酶 3(PR3)为阴性,但当全身症状出现时转为阳性;另 2 例患者 PR3 阳性。3 例患者均有明显的面部病变。所有患者对抗生素或 PG 常用药物(包括皮质类固醇和环孢素)的治疗均无反应。所有患者对利妥昔单抗均有良好的反应。对电子数据库文献进行了回顾,共发现 4 例先前报道的病例。我们评估了以前报告的和我们新诊断的病例的临床特征、血清学和治疗反应。

结论

PG 样溃疡是儿科 GPA 的一种罕见表现,可能先于典型的系统性 GPA 症状出现。面部溃疡、皮肤活检的肉芽肿和中性粒细胞炎症以及对 PG 治疗无反应的特点是 GPA 相关性 PG 样溃疡的特征。我们的综述表明,利妥昔单抗治疗可能需要改善皮肤病变。认识到 PG 样溃疡可发生在儿科 GPA 中,可能会导致及时诊断、适当治疗和改善预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ec/8180159/1cdb00dd768d/12969_2021_564_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验