Results 21 to 30 of about 64,510,463 (206)
Rituximab-induced Acute Thrombocytopenia in Granulomatosis with Polyangiitis [PDF]
A 72-year-old Japanese woman diagnosed with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis was admitted to our hospital with hearing loss, temporal pain, and sudden blindness.
Shin-ya Kawashiri +37 more
core +1 more source
Granulomatosis with Polyangiitis (Wegener's): An alternative name for Wegener's Granulomatosis [PDF]
The Boards of Directors of the American College of Rheumatology, the American Society of Nephrology, and the European League Against Rheumatism recommend a gradual shift from honorific eponyms to disease-descriptive or etiology-based nomenclature.
Falk, R. J. +12 more
openaire +9 more sources
Objective: To determine the clinical and laboratory features during the disease course in patients of anti cytoplasmic antibody (ANCA) associated vasculitis in Pakistani patients presenting to a tertiary care center.
Muhammad Zeeshan Aslam +3 more
doaj +3 more sources
Accessory left gastric artery aneurysms in granulomatosis with polyangiitis : a case report and literature review [PDF]
2017-02Aneurysm formation is a potential complication of granulomatosis with polyangiitis (GPA), previously known as Wegener’s granulomatosis. It is a very rare complication, but immediate diagnosis and therapy should be performed because an aneurysm can
Hayashi, Shogo +12 more
core +1 more source
Primary pulmonary Hodgkin’s lymphoma (PPHL) is a rare subtype of lymphoma that comprises a small percentage of primary pulmonary lymphomas. Due to its rarity and nonspecific symptoms, PPHL often presents diagnostic challenges. This case report presents a
Julia Maria Sołek +6 more
core +1 more source
Granulomatosis with polyangiitis: rapidly progressive necrotizing glomerulonephritis in a pediatric patient [PDF]
Mariana Luna,1 Victoria Bocanegra,3 Patricia G Vallés1,21Nephrology Division, Pediatric Department, Dr Humberto Notti Pediatric Hospital, Mendoza, Argentina; 2Pathophysiology Area, Pathology Department, School of Medicine, National Cuyo University,
Bocanegra V, Vallés PG, Luna M
core +2 more sources
Background Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. Case presentation We report a case of eosinophilic
Alexandra C. Keefe +3 more
doaj +1 more source
Vascular thromboses with retroperitoneal fibrosis: a case report
Background Granulomatosis with polyangiitis is a systemic inflammatory disease characterized by necrotizing vasculitis that affects small- and medium-sized blood vessels.
Hanane Charaf +6 more
doaj +1 more source
Polyangiitis overlap syndrome of granulomatosis with polyangiitis (Wegener's granulomatosis) and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) [PDF]
Polyangiitis overlap syndrome is defined as systemic vasculitis that cannot be classified into one of the well-defined vasculitic syndromes. In this report, a female patient who presented with vasculitis-like and asthmatic symptoms was diagnosed as having polyangiitis overlap syndrome of granulomatosis with polyangiitis (GPA; formerly known as Wegener ...
Hironori, Uematsu +3 more
openaire +2 more sources
Granulomatosis with polyangiitis in Tunisia
Granulomatosis with polyangiitis (GPA) is more frequent in Northern rather than Southern countries. Very few studies have been conducted in Africa. We have performed a retrospective descriptive study including clinical and laboratory profiles of 30 Tunisian GPA patients seen at the department of Internal Medicine of the University Hospital of la Rabta ...
I. Ben Ghorbel +4 more
openaire +3 more sources

