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本文引用的文献

1
Allogeneic haematopoietic stem-cell transplantation for children with refractory systemic juvenile idiopathic arthritis and associated lung disease: outcomes from an international, retrospective cohort study.异基因造血干细胞移植治疗难治性全身型幼年特发性关节炎及相关肺部疾病患儿:一项国际回顾性队列研究的结果
Lancet Rheumatol. 2025 Apr;7(4):e243-e251. doi: 10.1016/S2665-9913(24)00275-3. Epub 2024 Dec 20.
2
Tracheobronchomalacia is common in children with primary ciliary dyskinesia-A case note review.先天性纤毛运动障碍患儿中气管支气管软化症很常见——病例报告
Pediatr Pulmonol. 2024 Dec;59(12):3560-3568. doi: 10.1002/ppul.27262. Epub 2024 Sep 18.
3
Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia.全基因组测序提高了原发性纤毛运动障碍的分子诊断水平。
Pediatr Pulmonol. 2024 Dec;59(12):3322-3332. doi: 10.1002/ppul.27200. Epub 2024 Aug 8.
4
Cyclosporine A in children with ABCA3 deficiency.ABCA3 缺陷患儿的环孢素 A。
Pediatr Pulmonol. 2024 Dec;59(12):3221-3227. doi: 10.1002/ppul.27178. Epub 2024 Jul 23.
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Serum biomarkers in neuroendocrine cell hyperplasia of infancy.婴儿期神经内分泌细胞增生症的血清生物标志物。
Pediatr Pulmonol. 2024 Nov;59(11):2885-2890. doi: 10.1002/ppul.27148. Epub 2024 Jun 27.
6
Detection of Bronchiolitis Obliterans Syndrome after Pediatric Hematopoietic Stem Cell Transplantation: An Official American Thoracic Society Clinical Practice Guideline.儿童造血干细胞移植后闭塞性细支气管炎综合征的检测:美国胸科学会临床实践指南。
Am J Respir Crit Care Med. 2024 Aug 1;210(3):262-280. doi: 10.1164/rccm.202406-1117ST.
7
Health-related quality scores in childhood interstitial lung disease: Good agreement between patient and caregiver reports.儿童间质性肺疾病的健康相关生活质量评分:患者报告与照料者报告一致性良好。
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8
The original histopathologic description of neuroendocrine cell hyperplasia of infancy is not applicable to every patient with the disease.婴儿期神经内分泌细胞增生症最初的组织病理学描述并不适用于该病的每一位患者。
Pediatr Pulmonol. 2024 Nov;59(11):3016-3019. doi: 10.1002/ppul.27118. Epub 2024 Jun 5.
9
Persistent tachypnea of infancy, neuroendocrine cell hyperplasia of infancy, and pulmonary interstitial glycogenosis: "A3-Specific conditions of undefined etiology".婴儿持续性呼吸急促、婴儿期神经内分泌细胞增生症和肺间质糖原沉积症:“病因不明的A3特定病症”
Pediatr Pulmonol. 2024 Oct;59(10):2702-2707. doi: 10.1002/ppul.27102. Epub 2024 May 31.
10
Radiographic Outcomes in Pediatric Bronchiectasis and Factors Associated with Reversibility.小儿支气管扩张症的影像学结果及与可逆性相关的因素
Am J Respir Crit Care Med. 2024 Jul 1;210(1):97-107. doi: 10.1164/rccm.202402-0411OC.

《儿科肺病学》2024年回顾:罕见和弥漫性肺病

Pediatric Pulmonology 2024 Year in Review: Rare and Diffuse Lung Disease.

作者信息

Cheng Pi Chun, Liptzin Deborah R, Garagozlo Katiana, Barber Andrew T

机构信息

Division of Pediatric Pulmonology, Allergy, and Sleep Medicine, Riley Hospital for Children, Indianapolis, Indiana, USA.

Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

Pediatr Pulmonol. 2025 Apr;60(4):e71096. doi: 10.1002/ppul.71096.

DOI:10.1002/ppul.71096
PMID:40243387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12005123/
Abstract

The field of pediatric rare and diffuse lung diseases continues to advance, with ongoing research deepening our understanding of the diagnosis and treatment of conditions such as children's interstitial and diffuse lung disease (chILD), non-cystic fibrosis (CF) bronchiectasis, and pulmonary complications of childhood cancer. Recent publications in Pediatric Pulmonology and other journals in 2024 have highlighted new insights into the pathophysiology, disease progression, and emerging diagnostic tools for these rare lung conditions, as well as innovative therapeutic approaches. This review features these important advancements within the context of current diagnostic practices and clinical care for pediatric patients with rare and diffuse lung diseases.

摘要

儿科罕见和弥漫性肺部疾病领域不断发展,正在进行的研究加深了我们对儿童间质性和弥漫性肺部疾病(chILD)、非囊性纤维化(CF)支气管扩张以及儿童癌症肺部并发症等疾病的诊断和治疗的理解。2024年发表在《儿科肺病学》和其他期刊上的最新文章突出了对这些罕见肺部疾病的病理生理学、疾病进展、新兴诊断工具以及创新治疗方法的新见解。本综述在当前针对患有罕见和弥漫性肺部疾病的儿科患者的诊断实践和临床护理背景下介绍了这些重要进展。