Lung Transplant Recipient with Pulmonary Alveolar Proteinosis
Keyword(s):
Pulmonary alveolar proteinosis (PAP) is a progressive lung disease characterized by accumulated surfactant-like lipoproteinaceous material in the alveoli and distal bronchioles. This accumulation is the result of impaired clearance by alveolar macrophages. PAP has been described in 11 solid organ transplant recipients, 9 of whom were treated with mammalian target of rapamycin inhibitors. We report a case of a lung transplant recipient treated with prednisone, mycophenolate mofetil (MMF), and tacrolimus who ultimately developed PAP, which worsened when MMF was replaced with everolimus.
2019 ◽
Vol 59
(1)
◽
pp. 91-98
◽
1995 ◽
Vol 20
(3)
◽
pp. 617-620
◽
2020 ◽
Vol 28
(4)
◽
pp. 674-679