儿童风湿病中的炎症性肠病。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Özen Taş, Fatma Aydın, Zarife Kuloğlu, Ceyda Tuna Kırsaçlıoğlu, Onur Bahçeci, Betül Öksüz Aydın, Doğacan Sarısoy, Zeynep Birsin Özçakar
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引用次数: 0

摘要

儿童风湿病(RD)是在自身免疫或炎症基础上发生的全身性疾病,可伴有炎症性肠病(IBD)。当不了解这种关联时,所应用的治疗可能不充分,并且/或对RD给予的治疗甚至可能导致IBD结果的聚集。因此,早期识别关联对于疾病的正确管理至关重要。目的:本研究的目的是显示rd患者中IBD的频率。我们还旨在调查在哪些情况下应该怀疑患有rd的儿童患有IBD。方法:回顾性分析2012年至2024年在我院儿科风湿病科随访的诊断为RD并诊断为IBD的患者的电子病历。结果:2012 - 2024年,650例家族性地中海热(FMF)患者中有20例(3%),40例慢性非细菌性骨髓炎(CNO)患者中有3例(7.5%)(其中1例同时患有FMF), 170例青少年特发性关节炎(JIA)患者中有2例(1.2%)被诊断为IBD。15名(62.5%)患者接受RD作为初始诊断,其中9名(37.5%)患者最初诊断为IBD,然后因其症状转介到风湿病学。诊断为RD的中位年龄为9岁(四分位间距(IQR), 14.5)。诊断为IBD时的中位年龄为12岁(IQR, 13),其中12例(50%)患有克罗恩病(CD), 10例(41.6%)患有溃疡性结肠炎(UC), 2例(8.4%)患有不明疾病。虽然大多数患者具有IBD的典型表现,但有4例患者表现出更模糊的症状,包括难治性缺铁性贫血、肛周脓肿、体重减轻和生长迟缓。结论:RD与IBD具有相似的病理通路和临床表现,IBD可伴随多种RD,应在出现罕见和不典型症状时考虑IBD的诊断。此外,有复杂肠外症状的IBD患儿也应考虑RD。•RD,尤其是FMF、JIA和CNO,可能与IBD有关。•儿科风湿病学家应考虑在RD过程中出现非典型表现的IBD作为潜在的诊断。•RD和IBD的共存在疾病进展和治疗决策方面都很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inflammatory bowel disease in paediatric rheumatological diseases.

Introduction: Rheumatological diseases (RD) in childhood are systemic diseases that occur on the basis of auto-immunity or inflammation, and they can be accompanied by inflammatory bowel disease (IBD). When there is no knowledge of this association, the treatments applied may not be sufficient and/or treatments given for RD may even lead to aggrevation of IBD findings. Thus, early identification of an association is crucial for the correct management of the diseases.

Objectives: The aim of this study is to show the frequency of IBD in patients with RDs. We also aimed to investigate in which cases IBD should be suspected in children with RDs.

Methods: Electronic medical records of the patients who were followed up between 2012 and 2024 with a diagnosis of RD in our Paediatric Rheumatology Unit and diagnosed with IBD were reviewed retrospectively.

Results: Between 2012 and 2024, 20 (3%) of 650 familial Mediterranean fever (FMF) patients, 3 (7.5%) of 40 chronic nonbacterial osteomyelitis (CNO) patients (one of them also had FMF) and 2 (1.2%) of 170 juvenile idiopathic arthritis (JIA) patients were diagnosed with IBD. While 15 (62.5%) of the patients received a RD as the initial diagnosis, 9 (37.5%) of them were initially diagnosed with IBD and then referred to rheumatology for their symptoms. The median age at the diagnosis of RD was 9 years (inter quartile range (IQR), 14.5). The median age at the diagnosis of IBD was 12 years (IQR, 13), and 12 patients (50%) had Crohn's disease (CD), 10 patients (41.6%) ulcerative colitis (UC) and 2 patients (8.4%) undeterminated disease. Although majority of the patients had classical findings of IBD, 4 patients presented with more vague symptoms including treatment-resistant iron deficiency anaemia, perianal abscess, weight loss and growth retardation.

Conclusions: RD and IBD share similar pathological pathways and clinical findings, and IBD can accompany to various RD. The diagnosis of IBD should be considered in the presence of rare and atypical symptoms. Furthermore, RD should also be considered in children with IBD who have complex extraintestinal symptoms. Key Points • RD, especially FMF, JIA and CNO, may be associated with IBD. • Paediatric rheumatologists should consider IBD as a potential diagnosis in the presence of atypical findings that may develop during the course of RD. • The co-existence of RD and IBD is important both in terms of disease progression and treatment decisions.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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