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Respiratory subtype of relapsing polychondritis frequently presents as difficult asthma: a descriptive study of respiratory involvement in relapsing polychondritis with 13 patients from a single UK centre

机译:复发多档炎的呼吸亚型经常存在困难的哮喘:呼吸涉及复发呼吸道患者的描述性研究,其中13名来自英国中心的13名患者

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摘要

IntroductionRelapsing polychondritis is a rare multisystem vasculitis characterised by recurrent cartilage inflammation. Respiratory involvement, of which tracheobronchomalacia (TBM) is the commonest form, is difficult to treat and is linked to increased mortality. We describe 13 patients with respiratory involvement.MethodsThis is a retrospective study of all the patients with relapsing polychondritis at University Hospitals Coventry and Warwickshire NHS Trust (UHCW), a secondary care provider for ∼500 000. Only patients with respiratory involvement were included in this study.ResultsWe identified 13 patients who fulfilled the inclusion criteria. Most patients were identified from the “difficult asthma” clinic. TBM was seen in 11 patients, whilst two patients had pleural effusions which resolved with immunosuppression and one patient had small airways disease. Computed tomography scans (inspiratory and expiratory) and bronchoscopy findings were useful in diagnosing TBM. Pulmonary function testing revealed significant expiratory flow abnormalities. All patients were treated with corticosteroids/disease-modifying anti-rheumatic drugs (DMARDs) and some were given cyclophosphamide or biological agents, although the response to cyclophosphamide (1 out of 4) or biologicals (2 out of 4) was modest in this cohort. Ambulatory continuous positive airway pressure ventilation was successful in four patients.ConclusionsRelapsing polychondritis may be overlooked in “difficult asthma” clinics with patients having TBM (not asthma) and other features of relapsing polychondritis. Awareness of this condition is crucial to enable early diagnosis and interventions to reduce the risk of life-threatening airway collapse. A number of patients respond well to DMARDs and are able to minimise corticosteroid use.
机译:引入多晶体炎是一种罕见的多系统血管炎,其特征是通过复发软骨炎症。呼吸受累,其中气管龙肿瘤(TBM)是最常见的形式,难以治疗并与增加的死亡率相关联。我们描述了13名呼吸患者患有呼吸道的患者.THISTHIS是对大学医院COVENTRY和WARWICKSHIRE NHS TRUST(UHCW)复发多档炎患者的回顾性研究,是〜500 000的二级护理提供者。只有呼吸道参与患者学习。鉴定13名符合纳入标准的13名患者。大多数患者被鉴定在“困难的哮喘”诊所中鉴定出来。在11名患者中观察到TBM,虽然两名患者有胸膜湿度,用免疫抑制和一名患者进行了小型气道疾病。计算的断层扫描扫描(吸气和呼气)和支气管镜检查在诊断TBM方面是有用的。肺功能检测显示出现明显的呼气流异常。所有患者均用皮质类固醇/疾病改性抗风湿药物(DMARDS)治疗,有些是给予环磷酰胺或生物制剂,尽管对环磷酰胺(1个)或生物学(2个中的1个)的反应在这种队列中适度。动态连续正气道压力通风在四名患者中成功。与患有TBM(不是哮喘)的患者和复发多档炎的其他特征,可以忽略聚氯膜炎的链接。对这种情况的认识至关重要,以实现早期诊断和干预,以降低危及生命的气道崩溃的风险。许多患者对DMARD响应并能够最大限度地减少皮质类固醇使用。

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