Late-Onset Exudative Pleural Effusions Without Concomitant Airway Obstruction or Lung Parenchymal Abnormalities: A Novel Presentation of Chronic Lung Allograft Dysfunction.
Devika SinduSandhya BansalBhuvin BuddhdevKendra McAnallyHesham MohamedRajat WaliaThalachallour MohanakumarSofya TokmanPublished in: Transplant international : official journal of the European Society for Organ Transplantation (2024)
Restrictive allograft syndrome (RAS) is an aggressive variant of CLAD characterized by progressive restrictive ventilatory decline and persistent pleuro-parenchymal changes that can be seen on chest CT. We identified four lung transplant recipients with a progressive restrictive ventilatory defect due to lymphocyte-predominant exudative pleural effusions, but no pleuro-parenchymal abnormalities typical of RAS. Using molecular analysis, we also found increased levels of previously described immune markers of RAS, including NFkB, 20S proteasome, lipocalin, TNFα, and TGFβ, within the circulating small extracellular vesicles of the remaining living lung transplant recipient. Despite the absence of lung parenchymal changes, these patients had a poor prognosis with rapid deterioration in allograft function and no response to pleural-based interventions such as thoracentesis, decortication, and pleurodesis. We hypothesize that these cases represent a distinct CLAD phenotype characterized by progressive restriction due to pleural inflammation, lymphocyte-predominant pleural effusion, resultant compressive atelectasis, and eventual respiratory failure in the absence of lung parenchymal involvement.
Keyphrases
- poor prognosis
- late onset
- multiple sclerosis
- oxidative stress
- long non coding rna
- end stage renal disease
- rheumatoid arthritis
- early onset
- newly diagnosed
- chronic kidney disease
- magnetic resonance imaging
- computed tomography
- case report
- extracorporeal membrane oxygenation
- peripheral blood
- magnetic resonance
- kidney transplantation
- epithelial mesenchymal transition
- transforming growth factor
- intensive care unit
- positron emission tomography
- soft tissue