儿童血管炎的人口统计学和临床特征:一项单中心研究。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY
ARP Rheumatology Pub Date : 2023-01-01
Tiago Santos Trindade, Catarina Granjo Morais, Ana Maia, Mariana Rodrigues, Iva Brito
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引用次数: 0

摘要

血管性疾病是一种罕见的全身性疾病,可能发生在儿童时期。本研究旨在记录一个三级中心的全身性血管病的人口学和临床特征,并将我们的结果与其他国际中心先前发表的研究结果进行比较。方法:从2009年到2020年,18岁前出现全身性血管炎的患者,在诊断或随访期间入住葡萄牙三级中心,回顾性纳入本研究。结果:在我们的研究中,我们纳入138例患者。诊断时最年轻的患者为川崎病(KD)组,诊断时中位年龄为2.26岁(IQR 1.07-6.20),而behet综合征(BS)组诊断时中位年龄为13.41岁(IQR 10.19-16.75), IgA血管炎(IgAV)和KD的中位年龄均显著高于川崎病(IQR 10.19-16.75) (p < 90%)。胃肠道症状在所有组中都很常见(15-50%),BS组较少见(17%)。关节炎和关节痛在IgAV中非常普遍(65%)。62%的病例符合美国心脏协会诊断完全KD的标准。完全诊断与不完全诊断的年龄分布差异无统计学意义(p=0.616)。患者平均发热时间9.6±2.1 d,高于预期。IgAV患者的肾脏表现(11%)和BS患者的眼部受累(22%)低于预期。有显著数量的儿童报告共同参与KD(27%)。我们还注意到BS中血管事件的发生率略高(30%)。结论:评估的每种特定血管炎有不同的关键症状,但我们的患者有几种主诉和体征,其中一些与血管炎重叠,另一些非常不典型,如BS患者因微血管炎引起的复发性附睾炎。我们可以说,我们的大多数发现都与当前的文献一致,但也有一些明显的例外。儿科多中心人群为基础的研究是必要的,以增加研究和设计有关这一知识领域的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Demographic and clinical features of pediatric vasculitis: a single-center study.

Introduction: Vasculitides are rare systemic conditions which may occur in childhood. This study aims to document demographic and clinical features of systemic vasculitides in a tertiary center, comparing our outcomes with previously published studies of other international centers.

Methods: Patients presenting with systemic vasculitis before 18 years of age, admitted to a tertiary Portuguese center at diagnosis or during follow-up, from 2009 to 2020, were retrospectively included in this study.

Results: In our study, we included 138 patients. The youngest patients at diagnosis were in the Kawasaki's disease (KD) group, with a median age at diagnosis of 2.26 years old (IQR 1.07-6.20), as opposed to the Behçet's syndrome (BS) group with a median age at diagnosis of 13.41 years old (IQR 10.19-16.75), which was significantly higher (p 90% in both IgA Vasculitis (IgAV) and KD. Gastrointestinal symptoms were common in all groups (15-50%), rarer in BS (17%). Arthritis and arthralgia were highly prevalent in IgAV (65%). The American Heart Association criteria of diagnosis for complete KD were met in 62% of cases. No significant difference was found in age distribution between complete and incomplete diagnosis (p=0.616). Mean duration of fever in KD was 9.6 ±2.1 days, which was higher than anticipated. Renal manifestations in IgAV (11%) and ophthalmic involvement in BS (22%) were lower than expected. There was a notable number of children reporting joint involvement in KD (27%). We also noticed a slightly higher prevalence of vascular events in BS (30%).

Conclusions: Each specific vasculitis assessed had different key symptoms, but there are several complaints and signs shown by our patients, some of them overlapping between vasculitides and others very atypical, such as recurrent epididymitis in BS due to microvasculitis. We can state that most of our findings are in concordance with current literature, with some notable exceptions. Pediatric multicentric population-based studies are warranted to increase research and design clinical trials concerning this field of knowledge.

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