Search
Search Results
-
Management of granulomatosis with polyangiitis complicated by intestinal perforation and pancytopenia: a case report and literature review
Granulomatosis with polyangiitis is a systemic vasculitis. While the classic triad typically comprises otorhinolaryngologic, pulmonary, and renal...
-
Pituitary hypophysitis in granulomatosis with polyangiitis (GPA): a case series
Granulomatosis with polyangiitis (GPA) rarely involves the pituitary gland. Pituitary involvement has been reported in ~ 1% of all cases of GPA. Most...
-
Clinical implications of peripheral eosinophil count at diagnosis in patients newly diagnosed with microscopic polyangiitis and granulomatosis with polyangiitis
BackgroundThis study investigated the clinical implications of peripheral eosinophil count at diagnosis in estimating cross-sectional antineutrophil...
-
Circulating cold-inducible RNA-binding protein levels in microscopic polyangiitis and granulomatosis with polyangiitis
ObjectiveThis study investigated whether circulating cold-inducible RNA-binding protein (CIRP) could be a biomarker to reflect the current activity,...
-
Peripheral T-cell lymphoma mimicking granulomatosis with polyangiitis
Upper respiratory tract involvement is common in patients with granulomatosis with polyangiitis (GPA), but malignancies should be kept in mind in the...
-
A case of rapid avacopan-induced liver injury in pediatric granulomatosis with polyangiitis
Children with anti-neutrophil cytoplasmic antibody-associated vasculitis benefit immensely from avacopan as it reduces the requirement for steroids....
-
Limited Granulomatosis With Polyangiitis of Nose and Paranasal Sinuses – a Case Report
Granulomatosis with polyangiitis is a rare disease with involvement of multiple organ system. It classically affects the upper respiratory tract,...
-
Unilateral diaphragmatic palsy and pleuropericarditis in a patient with granulomatosis with polyangiitis: a case report
BackgroundGranulomatosis with polyangiitis (GPA) is a rare small vessel vasculitis predominantly affecting upper and lower respiratory tract and...
-
Massive, life-threatening hemoptysis due to localized granulomatosis with polyangiitis
Massive hemoptysis may be related to a wide spectrum of diseases whose differential diagnosis can be challenging, also due to the medical emergency...
-
Clinical characteristics of hypertrophic cranial pachymeningitis in granulomatosis with polyangiitis: a retrospective single-center study in China
BackgroundHypertrophic cranial pachymeningitis (HCP) is uncommon but a poorly understood complication of granulomatosis with polyangiitis (GPA).
... -
Granulomatosis with polyangiitis presenting as a solitary renal mass: a case report
BackgroundGranulomatosis with polyangiitis (GPA) is characterized by necrotizing granulomatous vasculitis involving small-sized vessels in the upper...
-
Evidence-Based Guideline for the diagnosis and management of eosinophilic granulomatosis with polyangiitis
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, characterized by...
-
Eosinophilic granulomatosis with polyangiitis and its association with montelukast: a case-based review
The association between the use of certain medications (including sulfonamides, hydralazine, and procainamide) and the occurrence of drug-induced...
-
A Review of Anti-IL-5 Therapies for Eosinophilic Granulomatosis with Polyangiitis
Eosinophilic granulomatosis with polyangiitis (EGPA), previously known as Churg–Strauss syndrome, is a systemic disorder characterized by asthma,...
-
Updates of ocular involvement in granulomatosis with polyangiitis
Granulomatosis with polyangiitis (GPA) is a systemic inflammatory disease characterized by necrotizing vasculitis of the small-to-medium-sized...
-
Successful treatment with rituximab and plasmapheresis of renal involvement of eosinophilic granulomatosis with polyangiitis
BackgroundEosinophilic granulomatosis with polyangiitis (EGPA) is a rare disorder characterized by asthma, eosinophilia, and systemic vasculitis....
-
Ocular manifestations of granulomatosis with polyangiitis: report from a tertiary eye care center
PurposeTo report demographic characteristics and ophthalmological manifestations of patients with granulomatosis with polyangiitis (GPA) in a...
-
Testicular vasculitis in eosinophilic granulomatosis with polyangiitis: a case-based review
Testicular vasculitis (TV) develops when an organ is involved in systemic vasculitis. A 47-year-old man with eosinophilic granulomatosis with...
-
Lung cancer in older patients with granulomatosis with polyangiitis: a report of three cases
BackgroundGranulomatosis with polyangiitis (GPA) is characterized by necrotizing granulomatous inflammation with necrotizing vasculitis predominantly...
-
Limited granulomatosis with polyangiitis in children with idiopathic orbital inflammation: a case series and literature review
Idiopathic orbital inflammation (IOI) is a diagnosis of exclusion, but the exclusion of other inflammatory diseases of the orbit is broad and relies...