Peer-reviewedCC BY-NCERJ Open Research
No detectable infectious agents in Langerhans cell histiocytosis with lung involvement
Abstract
Extract Langerhans cell histiocytosis (LCH) is a rare neoplastic disease of unknown aetiology driven by various somatic mutations in the mitogen-activated protein kinase (MAPK) pathway [1]. LCH is highly heterogeneous and may affect virtually any organ [2]. Lung involvement is frequently observed in adult LCH patients, almost exclusively in young smokers of both sexes [3].
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BibTeX
@article{salmona2026detectable,
title = {{No detectable infectious agents in Langerhans cell histiocytosis with lung involvement}},
author = {Maud Salmona and Amira Benattia and Véronique Meignin and Valentine Marie Ferré and Fanélie Jouenne and Gwenaël Lorillon and Jerôme Le Goff and Samia Mourah and Abdellatif Tazi},
journal = {ERJ Open Research},
year = {2026},
month = jul,
doi = {10.1183/23120541.01689-2025},
url = {https://hal.science/hal-05782789v1},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - No detectable infectious agents in Langerhans cell histiocytosis with lung involvement
AU - Maud Salmona
AU - Amira Benattia
AU - Véronique Meignin
AU - Valentine Marie Ferré
AU - Fanélie Jouenne
AU - Gwenaël Lorillon
AU - Jerôme Le Goff
AU - Samia Mourah
AU - Abdellatif Tazi
PY - 2026
DA - 2026/07/16
JO - ERJ Open Research
DO - 10.1183/23120541.01689-2025
UR - https://hal.science/hal-05782789v1
AB - Extract Langerhans cell histiocytosis (LCH) is a rare neoplastic disease of unknown aetiology driven by various somatic mutations in the mitogen-activated protein kinase (MAPK) pathway [1]. LCH is highly heterogeneous and may affect virtually any organ [2]. Lung involvement is frequently observed in adult LCH patients, almost exclusively in young smokers of both sexes [3].
SN - 2312-0541
ER -