| Literature DB >> 32511892 |
Olive S Eckstein1,2, Jed G Nuchtern3,4, George B Mallory5, R Paul Guillerman6, Matthew A Musick7, Mhairi Barclay8, Jayesh M Bhatt8, Patrick Davies9, Richard G Grundy10, Alice Martin11, Tom Hilliard12, Stephen P Lowis13, Susan Picton14, Vasanta Nanduri15, Johannes Visser16, Carl E Allen1,2, Kenneth L McClain1,2.
Abstract
Patients with pulmonary Langerhans cell histiocytosis (LCH) typically have a benign course but may have extensive cystic lung disease with rare life-threatening complications including multiple and recurrent pneumothoraces and respiratory failure. We report seven severely affected pediatric patients treated with chemotherapy, aggressive chest tube management, and pleurodesis of whom five survived. Patients with extraordinary amounts of pulmonary cystic disease and multiple pneumothoraces due to LCH can have remarkable, curative outcomes with early recognition, optimal LCH-directed therapy, and supportive care.Entities:
Keywords: Langerhans cell histiocytosis; chemotherapy; cystic lung disease; pleurodesis; pneumothorax
Mesh:
Year: 2020 PMID: 32511892 PMCID: PMC7771630 DOI: 10.1002/ppul.24822
Source DB: PubMed Journal: Pediatr Pulmonol ISSN: 1099-0496