Secondary pulmonary alveolar proteinosis
Synonyms: Secondary PAP
A rare acquired interstitial lung disease characterized by alveolar surfactant accumulation cough progressive dyspnea and respiratory insufficiency. The disease may be secondary to hematological disorder toxic inhalation and infection or may occur within the setting of immunosuppression after transplantation.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
Newly diagnosed with
Secondary pulmonary alveolar proteinosis?
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Breathe Support Network
MISSION STATEMENT The Breathe Support Networks mission is to provide support and education for pulmonary fibrosis patients and their families, helping them to better #LIVEwithPF. This includes, but is not limited to: - education about pulmonary fibrosis - guiding patients and families on how to talk to their healthcare team - providing tips to live a healthier more productive life - providing information about other pulmonary fibrosis resources
Help Hope Live
Help Hope Live assists individuals living with catastrophic injuries and illnesses to fundraise toward their medical expenses and related costs.
For a list of clinical trials in this disease area, please click here.