Spontaneous resolution of cryptogenic organizing pneumonia in pediatrics: A case report

Abi-Khalil, S.; Fadel, Nadya Ben; Menassa-Moussa, L.; Torbey, Paul-Henri; Haddad-Zébouni, S.

doi:10.1016/j.arcped.2016.02.021

Cited by 2 publications

(1 citation statement)

References 13 publications

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“…The differential tomographic diagnosis includes lymphoma, eosinophilic lung diseases, vasculitis, and sarcoidosis [3]. There are cases described with spontaneous resolution [19], but immunosuppresive pharmacotherapy has been reported to be useful in intersticial lung deseases in child [2] as in our case.…”

Section: Discussionmentioning

confidence: 89%

Criptogenic Organizing Pneumonia: A Case Report

Galeana¹,

Flores²,

Tellez³

et al. 2020

BJSTR

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Introduction:The cryptogenic organizing pneumonia (COP) forms part of the interstitial lung diseases that are rare in pediatrics. Clinical case:We report the case of a six-month-old female infant with respiratory symptoms of 2 months of evolution after a lower respiratory tract infection. The clinical, radiologic and histopathologic correlations are presented. Conclusion:The COP is uncommon in pediatrics; therefore, the proper approach during the admission helps us to differentiate from other interstitial diseases that are difficult to diagnose at this age.

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Section: Discussionmentioning

confidence: 89%

Criptogenic Organizing Pneumonia: A Case Report

Galeana¹,

Flores²,

Tellez³

et al. 2020

BJSTR

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ERS statement on transition of care in childhood interstitial lung diseases

Pohunek,

Manali,

Vijverberg

et al. 2024

Eur Respir J

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Interstitial lung diseases (ILD) are a heterogeneous group of rare diffuse diseases affecting the lung parenchyma in children and adults. Childhood interstitial lung diseases (chILD) are often diagnosed at very young age, affect the developing lung, and can have different presentations and prognosis compared to adult forms of these diseases. Also, chILD in many cases may apparently remit, and have a better response to therapy and better prognosis than adult ILD. Many affected children will reach adulthood with minimal activity or clinical remission of the disease. They need continuing care and follow-up from childhood to adulthood if the disease persists and progresses over time but also if they are asymptomatic and in full remission. Therefore, for every chILD patient an active transition process from paediatric to adult care should be guaranteed. This ERS statement provides a review of the literature and current practice concerning transition of care in chILD. It draws on work in existing transition care programs in other chronic respiratory diseases, disease-overarching transition of care programs, evidence on the impact of these programs on clinical outcomes, current evidence regarding long-term remission of chILD as well as the lack of harmonisation between the current adult ILD and chILD classifications impacting on transition of care. While the transition system is well established in several chronic diseases, such as cystic fibrosis or diabetes mellitus, we could not find sufficient published evidence on transition systems in chILD. This statement summarises current knowledge but cannot yet provide evidence-based recommendations for clinical practice.

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Spontaneous resolution of cryptogenic organizing pneumonia in pediatrics: A case report

Cited by 2 publications

References 13 publications

Criptogenic Organizing Pneumonia: A Case Report

Criptogenic Organizing Pneumonia: A Case Report

ERS statement on transition of care in childhood interstitial lung diseases

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