词条 | Pulmonary-renal syndrome |
释义 |
CausesPulmonary-renal syndromes are most commonly caused by an underlying autoimmune disease. PRS is most commonly due to ANCA-associated vasculitides (e.g., granulomatosis with polyangiitis) or due to anti-basement membrane diseases (e.g., Goodpasture's syndrome). Granulomatosis with polyangiitis usually presents with nasopharyngeal involvement as well, whereas Goodpasture's will not. Microscopic polyangiitis is the most common cause of pulmonary-renal syndrome. Other causes include systemic lupus erythematosus, eosinophilic granulomatosis with polyangiitis, microscopic polyangiitis, dermatomyositis, polymyositis, mixed connective tissue disease, poststreptococcal glomerulonephritis, rheumatoid arthritis, and systemic sclerosis.[1] Less common causes also include IgA vasculitis and cryoglobulinemic vasculitis. Other etiologies include toxic injury such as paraquat poisoning, infection with hantavirus, leptospirosis, or legionella, or vascular, as seen in nephrotic syndrome when a renal vein thrombosis embolizes to the lungs. DiagnosisDifferential diagnosisCardiogenic shock can mimic a pulmonary renal syndrome and lead to coughing up blood due to pulmonary edema and kidney failure from inadequate blood flow.[1]Treatment is primarily by corticosteroids and immunosuppressive medications like cyclophosphamide, methotrexate, and azathioprine. Plasmapheresis can be used in some circumstances. References1. ^1 2 3 4 {{cite journal|last1=West|first1=SC|last2=Arulkumaran|first2=N|last3=Ind|first3=PW|last4=Pusey|first4=CD|title=Pulmonary-renal syndrome: a life threatening but treatable condition|journal=Postgraduate Medical Journal|date=May 2013|volume=89|issue=1051|page=274-83|doi=10.1136/postgradmedj-2012-131416|pmid=23349383|type=Review}} {{Respiratory pathology}}{{Urologic disease}}{{Hypersensitivity and autoimmune diseases}}{{respiratory-disease-stub}}{{genitourinary-disease-stub}} 2 : Lung disorders|Syndromes |
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