Pulmonary-renal syndrome: Difference between revisions
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== Background == |
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* Usually refers to a combination of [[glomerulonephritis]] and [[pulmonary hemorrhage]] |
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* Most common causes are [[ANCA-associated vaculitis]] and [[anti-GBM disease]] |
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== Differential Diagnosis == |
== Differential Diagnosis == |
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* [[ANCA-associated vaculitis|ANCA-associated small vessel vaculitis]] (70%) |
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** [[Granulomatosis with polyangiitis]] |
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* Small-vessel vasculitis (ANCA-associated) |
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** [[Eosinophilic granulomatosis with polyangiitis]] |
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** GPA |
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** [[Microscopic polyangiitis]] |
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** eGPA |
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** MPA |
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* Rarely |
* Rarely |
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** Cryoglobulinemic vasculitis |
** [[Cryoglobulinemic vasculitis]] |
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** Systemic lupus erythematosus |
** [[Systemic lupus erythematosus]] |
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** IgA vasculitis |
** [[IgA vasculitis]] |
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* Even more rare: [[thrombotic microangiopathy]], [[rheumatoid arthritis]], [[systemic sclerosis]], [[mixed connective tissue disease]], [[polymyositis]], and [[dermatomyositis]] |
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[[Category:Respirology]] |
[[Category:Respirology]] |
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[[Category:Nephrology]] |
[[Category:Nephrology]] |
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[[Category:Rheumatology]] |
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Latest revision as of 14:43, 12 December 2023
Background
- Usually refers to a combination of glomerulonephritis and pulmonary hemorrhage
- Most common causes are ANCA-associated vaculitis and anti-GBM disease
Differential Diagnosis
- ANCA-associated small vessel vaculitis (70%)
- Anti-GBM antibody disease (Goodpasture syndrome) (20%)
- Rarely
- Even more rare: thrombotic microangiopathy, rheumatoid arthritis, systemic sclerosis, mixed connective tissue disease, polymyositis, and dermatomyositis
