Immunoglobulin G4-related disease (IgG4-RD) is a rare systemic fibroinflammatory disease that can affect almost any organ in the body. The most common sites of IgG4-RD include the salivary glands, orbits and lacrimal glands, pancreas, biliary tree, retroperitoneum and thyroid. Immunoglobulin G4-related lung disease (IgG4-RLD) can occur in isolation or as a component of multisystem disease. Its manifestations are heterogeneous and include lung cavitation, interstitial changes, pleural effusions and lung lesions. We describe a patient with Ig4-RLD manifesting as bronchial stenosis and left upper lobe collapse.
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Hosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, Spain
Univ Western Ontario, Rheumatol Div, London, ON, Canada
Univ Western Ontario, Gen Internal Med Dept, Windsor Campus, Windsor, ON, CanadaHosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, Spain
Fernandez-Codina, Andreu
Orozco-Galvez, Olimpia
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Hosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, SpainHosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, Spain
Orozco-Galvez, Olimpia
Martinez-Valle, Fernando
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Hosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, SpainHosp Univ Vall dHebron, Gen Internal Med Dept, Syst Autoimmune Dis Unit, Passeig Vall dHebron 119-129, Barcelona 08035, Spain