Bronchiectasis in a patient with Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy: a case report.

IF 2.6 3区 医学 Q2 RESPIRATORY SYSTEM
Margherita S Silani, Edoardo Simonetta, Andrea Gramegna, Alessandro De Angelis, Francesco Blasi, Stefano Aliberti
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Abstract

Background: The rare monogenic syndrome Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) leads to multisystemic autoimmunity with possible lung involvement. Autoimmune pneumonitis is a rare manifestation, with bronchiectasis being the most frequent radiologic pattern, and may lead to fatal outcome. The Sardinian population in Italy has a high incidence of APECED, although no case of lung manifestation has been reported yet in this cohort. This is the case of a Sardinian APECED patient referred to a bronchiectasis clinic. Our aim is to raise awareness and screen these patients earlier for pulmonary involvement and to initiate multidisciplinary treatment for better outcome.

Case presentation: A 49-year-old female native of Sardinia from consanguineous parents was diagnosed with APECED in childhood and was referred to our bronchiectasis clinic in March 2023. In addition to typical APECED features, she reported recurrent respiratory infections since childhood, chronic purulent sputum and a hospitalization for pneumonia. She came to our attention with a recent isolation of P. aeruginosa on sputum culture and diffuse cylindrical and varicoid bronchiectasis on her first CT scan. She underwent aetiologic screening for bronchiectasis with no evidence of another cause of disease. Lung treatment was optimized according to bronchiectasis guidelines, and during follow-up the patient developed methicillin-resistant Staphylococcus aureus (MRSA) infection and M. intracellulare pulmonary disease. The patient was offered P. aeruginosa eradication treatment with intravenous antibiotics and initiation of antimycobacterial therapy.

Conclusion: This is the first documented lung involvement case of APECED in a Sardinian patient, and the first patient reported to enter a bronchiectasis program. The patient was prescribed lung imaging late in time when bronchiectasis complications were already present. Our case report highlights the need for early pulmonary screening and multidisciplinary management in patients with APECED.

一名自身免疫性多内分泌病-糜烂性表皮营养不良患者的支气管扩张症:病例报告。
背景:罕见的单基因综合征 "自身免疫性多内分泌病-念珠菌病-外胚层营养不良症(APECED)"会导致多系统自身免疫,并可能累及肺部。自身免疫性肺炎是一种罕见的表现,支气管扩张是最常见的放射学模式,并可能导致致命的后果。意大利的撒丁岛人是 APECED 的高发人群,但在这一人群中尚未有肺部表现的病例报道。这是一例转诊到支气管扩张诊所的撒丁岛 APECED 患者。我们的目的是提高人们的认识,更早地筛查这些患者的肺部受累情况,并启动多学科治疗,以获得更好的治疗效果:一名 49 岁的撒丁岛女性患者,父母为近亲结婚,童年时被诊断出患有 APECED,并于 2023 年 3 月转诊至我们的支气管扩张诊所。除了典型的 APECED 特征外,她还报告自童年起反复呼吸道感染、慢性化脓性痰,并曾因肺炎住院治疗。最近,她在痰培养中分离出铜绿假单胞菌,并在首次 CT 扫描中发现弥漫性圆柱形和曲张型支气管扩张,因此引起了我们的注意。她接受了支气管扩张症病因学筛查,没有发现其他病因。根据支气管扩张症指南对肺部治疗进行了优化,在随访期间,患者出现了耐甲氧西林金黄色葡萄球菌(MRSA)感染和粟粒肿肺病。患者接受了静脉注射抗生素根除铜绿假单胞菌的治疗,并开始接受抗霉菌治疗:这是撒丁岛首例记录在案的 APECED 肺部受累病例,也是首例进入支气管扩张计划的患者。患者在支气管扩张并发症已经出现时才接受肺部造影检查。我们的病例报告强调了对 APECED 患者进行早期肺部筛查和多学科管理的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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