Granulomatosis with polyangiitis (GPA) is a primary, systemic small vessel vasculitis. The respiratory tract is typically involved in the course of the disease. Abnormalities on the chest radiograph are noted in more than 70% patients at some point during their disease history. In some clinical situations it is difficult to distinguish whether symptoms result from the underlying disease or are a symptom of infection. In these clinical situations, chest computed tomography (CT) can be very useful. We present a patient with GPA localized mainly in the respiratory tract with sudden deterioration of the general state and new abnormalities revealed in the CT of the chest
Background: Granulomatosus with Polyangiitis (GPA) is an Anti-neutrophilic Cytoplasmic Antibodies (A...
Granulomatosis with polyangiitis (GPA) is a relatively rare necrotizing vasculitis belonging to the ...
Granulomatosis with polyangiitis (GPA) is a systemic disorder characterized by necrotizing vasculiti...
Granulomatosis with polyangiitis (GPA) is a necrotizing vasculitis of small and medium vessels with ...
Granulomatosis with polyangiitis (Wegener’s granulomatosis) is a systemic vasculitis that ...
Abstract Even in the absence of disease‐specific radiological signs of granulomatosis with polyangii...
The coronavirus disease 2019 (COVID-19) has recently been found to cause cutaneous vasculitis in pat...
Granulomatosis with polyangiitis (GPA) is characterized by necrotic vasculitis of the medium and sma...
Granulomatosis with polyangiitis (GPA) is a rare form of vasculitis. Multidisciplinary therapeutic a...
Background. Granulomatosis with polyangiitis (GPA) is an ANCA associated small vessel vasculitis cha...
Copyright © 2015 Noreen Nasir et al. This is an open access article distributed under the Creative C...
WOS: 000388193400006PubMed: 25860849Granulomatosis with polyangiitis (GPA, formerly Wegener's granul...
Background: Granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomatosis), in which pulm...
Granulomatosis with polyangitis (GPA) represents a rare cause of systemic vasculitis with relatively...
PubMed ID: 25860849Background: Granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomato...
Background: Granulomatosus with Polyangiitis (GPA) is an Anti-neutrophilic Cytoplasmic Antibodies (A...
Granulomatosis with polyangiitis (GPA) is a relatively rare necrotizing vasculitis belonging to the ...
Granulomatosis with polyangiitis (GPA) is a systemic disorder characterized by necrotizing vasculiti...
Granulomatosis with polyangiitis (GPA) is a necrotizing vasculitis of small and medium vessels with ...
Granulomatosis with polyangiitis (Wegener’s granulomatosis) is a systemic vasculitis that ...
Abstract Even in the absence of disease‐specific radiological signs of granulomatosis with polyangii...
The coronavirus disease 2019 (COVID-19) has recently been found to cause cutaneous vasculitis in pat...
Granulomatosis with polyangiitis (GPA) is characterized by necrotic vasculitis of the medium and sma...
Granulomatosis with polyangiitis (GPA) is a rare form of vasculitis. Multidisciplinary therapeutic a...
Background. Granulomatosis with polyangiitis (GPA) is an ANCA associated small vessel vasculitis cha...
Copyright © 2015 Noreen Nasir et al. This is an open access article distributed under the Creative C...
WOS: 000388193400006PubMed: 25860849Granulomatosis with polyangiitis (GPA, formerly Wegener's granul...
Background: Granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomatosis), in which pulm...
Granulomatosis with polyangitis (GPA) represents a rare cause of systemic vasculitis with relatively...
PubMed ID: 25860849Background: Granulomatosis with polyangiitis (GPA, formerly Wegener’s granulomato...
Background: Granulomatosus with Polyangiitis (GPA) is an Anti-neutrophilic Cytoplasmic Antibodies (A...
Granulomatosis with polyangiitis (GPA) is a relatively rare necrotizing vasculitis belonging to the ...
Granulomatosis with polyangiitis (GPA) is a systemic disorder characterized by necrotizing vasculiti...