A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Lung biopsy findings and pulmonary function in children after allogeneic hematopoietic stem cell transplantation; 
Tekijät: Ukonmaanaho, Elli-Maija; Kirjavainen, Turkka; Martelius, Laura; Lohi, Jouko; Karikoski, Riitta; Koskenvuo, Minna; Taskinen, Mervi
Kustantaja: Springer Nature
Julkaisuvuosi: 2026
Lehti: Pediatric Research
ISSN: 0031-3998
eISSN: 1530-0447
DOI: https://doi.org/10.1038/s41390-026-05057-6
Julkaisun avoimuus kirjaamishetkellä: Avoimesti saatavilla
Julkaisukanavan avoimuus : Osittain avoin julkaisukanava
Verkko-osoite: https://www.nature.com/articles/s41390-026-05057-6
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/526673123
Rinnakkaistallenteen lisenssi: CC BY
Rinnakkaistallennetun julkaisun versio: Kustantajan versio
Lisätietoja: The datasets generated during and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Background Pulmonary complications are a major cause of morbidity after allogeneic hematopoietic stem cell transplantation (HSCT). Late-onset non-infectious pulmonary complications (LONIPCs), especially bronchiolitis obliterans syndrome (BOS), are difficult to diagnose, particularly in paediatric patients.
Methods In this retrospective single-center study, 14 of 325 paediatric HSCT recipients (4.3%) who developed severe pulmonary symptoms between 1999 and 2016 were analyzed. Lung biopsies were correlated with high-resolution computed tomography (HRCT) and pulmonary function tests (PFTs). Fourteen postmortem biopsies from HSCT patients without pulmonary symptoms served as controls.
Results Histology showed BOS in eight patients, cryptogenic organizing pneumonia (COP) in three, and interstitial fibrosis in three. None of the controls had findings suggestive of LONIPCs. All patients with BOS exhibited obstructive spirometry results, while restrictive changes occurred in COP and fibrosis. HRCT findings, including bronchial wall thickening and dilation, were frequent but non-specific. The incidence of LONIPCs and BOS was 4% and 2%, respectively.
Conclusions BOS was the most common late-onset pulmonary complication after paediatric HSCT. Obstructive PFT changes correlated well with histological BOS, whereas HRCT findings lacked specificity. Regular pulmonary function monitoring appears more reliable than imaging for early detection and may help prevent progression to irreversible lung disease.
Impact
This study highlights the diagnostic value of combining functional and histological assessment in children after HSCT.
Underscores the limitations of HRCT in detecting early BOS.
Supports routine pulmonary function surveillance as a non-invasive strategy to improve long-term outcomes.
Ladattava julkaisu This is an electronic reprint of the original article. |
Julkaisussa olevat rahoitustiedot:
1 Finnish Paediatric Cancer Foundation Väre, grant number 202100001, info@vareensaatio.fi. 2. Finnish Paediatric Research Foundation, grant number 200166, lts@lastentautientutkimussaatio.fi. Open Access funding provided by University of Helsinki (including Helsinki University Central Hospital).