Bridges Catherine, Shenk Mary Elizabeth Reed, Martin Kari, Launhardt Alison
Department of Pediatrics, Children's Mercy Kansas City, Kansas City, Missouri.
Department of Internal Medicine, Iowa Methodist Medical Center, Des Moines, Iowa.
Pediatr Dermatol. 2020 Jul;37(4):604-612. doi: 10.1111/pde.14144. Epub 2020 Mar 24.
BACKGROUND/OBJECTIVES: This study seeks to better define the clinical presentation and histopathology of cutaneous manifestations in childhood eosinophilic granulomatosis with polyangiitis (cEGPA).
Case reports were collected from Ovid Medline Database and PubMed using keyword identifiers from 1946 to 2017. Adult patients ≥ 18 years and cases not diagnosed with EGPA by the author were excluded. Sixty-five case reports of cEGPA were initially identified. These were reviewed individually, and fifty cases were determined to meet the American College of Rheumatology criteria for EGPA. No case series examining the cutaneous morphology and histopathology were identified. Cutaneous morphology, lesion location, and cutaneous histopathology results were recorded. Results were analyzed using summary statistics.
Sixty-four percent (32/50) of cEGPA patients presented with cutaneous manifestations. Twenty-nine cases provided specific morphological descriptions and lesion location. Common manifestations included purpura (15/29), subcutaneous nodules (8/29), and a macular/papular/maculopapular rash (8/29). However, twelve different cutaneous morphologies were identified in this review. Lesions occurred most commonly on the extremities (26/29). Twenty-two cases reported corresponding cutaneous histopathology, which revealed extravascular eosinophils (15/22), vasculitis (13/22), and granulomas (5/22). Only one biopsy sample (1/22) had all three classical EGPA characteristics of granulomas, extravascular eosinophils, and vasculitis.
With nearly two-thirds of cEGPA patients presenting with cutaneous manifestation, this study highlights the importance of clinical recognition of this disease by dermatologists. While the varied morphology of skin lesions and rarity of this disease makes cEGPA a difficult diagnosis, prompt recognition and treatment will improve outcomes in this patient population.
背景/目的:本研究旨在更明确儿童嗜酸性肉芽肿性多血管炎(cEGPA)皮肤表现的临床表现和组织病理学特征。
使用关键词标识符从1946年至2017年在Ovid Medline数据库和PubMed中收集病例报告。排除年龄≥18岁的成年患者以及作者未诊断为EGPA的病例。最初识别出65例cEGPA病例报告。对这些报告进行逐一审查,确定其中50例符合美国风湿病学会的EGPA标准。未发现研究皮肤形态学和组织病理学的病例系列。记录皮肤形态、病变部位和皮肤组织病理学结果。使用汇总统计数据进行结果分析。
64%(32/50)的cEGPA患者有皮肤表现。29例提供了具体的形态学描述和病变部位。常见表现包括紫癜(15/29)、皮下结节(8/29)和斑疹/丘疹/斑丘疹皮疹(8/29)。然而,本综述中识别出12种不同的皮肤形态。病变最常发生在四肢(26/29)。22例报告了相应的皮肤组织病理学检查结果,显示血管外嗜酸性粒细胞(15/22)、血管炎(13/22)和肉芽肿(5/22)。只有一个活检样本(1/22)具有肉芽肿、血管外嗜酸性粒细胞和血管炎这三种EGPA的经典特征。
近三分之二的cEGPA患者有皮肤表现,本研究强调了皮肤科医生对该病进行临床识别的重要性。虽然皮肤病变形态多样且该病罕见,使得cEGPA难以诊断,但及时识别和治疗将改善该患者群体预后。