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儿童间质性肺疾病的弥漫性肺泡出血:确定病因!

Diffuse alveolar hemorrhage in children with interstitial lung disease: Determine etiologies!

机构信息

Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-University (LMU) Munich, Munich, Germany.

Department of Pediatrics, Pediatric Pulmonology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.

出版信息

Pediatr Pulmonol. 2023 Apr;58(4):1106-1121. doi: 10.1002/ppul.26301. Epub 2023 Jan 13.

Abstract

OBJECTIVE

Diffuse alveolar hemorrhage (DAH) in children is a rare condition resulting from different underlying diseases. This study aimed at describing characteristics and diagnostic measures in children with ILD (children's interstitial lung disease, chILD) and DAH to improve the diagnostic approach by increasing clinician's awareness of diagnostic shortcomings.

PATIENTS AND METHODS

A retrospective data analysis of patients with ILD and DAH treated in our own or collaborating centers between 01/07/1997 and 31/12/2020 was performed. Data on clinical courses and diagnostic measures were systematically retrieved as case-vignettes and investigated. To assess suitability of diagnostic software-algorithms, the Human Phenotype Ontology (HPO) was revised and expanded to optimize conditions of its associated tool the "Phenomizer."

RESULTS

For 97 (74%) of 131 patients, etiology of pulmonary hemorrhage was clarified. For 34 patients (26%), no underlying condition was found (termed as idiopathic pulmonary hemorrhage, IPH). Based on laboratory findings or clinical phenotype/comorbidities, 20 of these patients were assigned to descriptive clusters: IPH associated with autoimmune features (9), eosinophilia (5), renal disease (3) or multiorgan involvement (3). For 14 patients, no further differentiation was possible.

CONCLUSION

Complete and sometimes repeated diagnostics are essential for establishing the correct diagnosis in children with DAH. We suggest assignment of patients with IPH to descriptive clusters, which may also guide further research. Digital tools such as the Phenomizer/HPO are promising, but need to be extended to increase diagnostic accuracy.

摘要

目的

弥漫性肺泡出血(DAH)在儿童中较为罕见,是由不同基础疾病引起的。本研究旨在描述ILD(儿童间质性肺病,chILD)和 DAH 患儿的特征和诊断方法,通过提高临床医生对诊断不足的认识,改善诊断方法。

患者和方法

对 1997 年 7 月 1 日至 2020 年 12 月 31 日期间在我们自己或合作中心治疗的ILD 和 DAH 患儿进行回顾性数据分析。系统地检索了病例的临床病程和诊断措施的数据,并进行了研究。为了评估诊断软件算法的适用性,对人类表型本体(HPO)进行了修订和扩展,以优化其相关工具“Phenomizer”的条件。

结果

131 例患儿中,97 例(74%)明确了肺出血的病因。34 例(26%)患儿未发现基础疾病(称为特发性肺出血,IPH)。根据实验室发现或临床表型/合并症,其中 20 例患儿被归为描述性聚类:与自身免疫特征相关的 IPH(9 例)、嗜酸性粒细胞增多症(5 例)、肾脏疾病(3 例)或多器官受累(3 例)。14 例患儿无法进一步区分。

结论

对 DAH 患儿进行全面且有时需重复的诊断对于确定正确的诊断至关重要。我们建议将 IPH 患儿归为描述性聚类,这也可能指导进一步的研究。数字工具如 Phenomizer/HPO 很有前途,但需要扩展以提高诊断准确性。

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