Results 51 to 60 of about 64,510,463 (206)
Orphanet Journal of Rare Diseases, 2016 Background The data from cohorts of childhood-onset granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) remain scarce and heterogeneous. We aimed to analyse the features at presentation, therapeutic approaches and the disease course
Michele Iudici +5 more
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Granulomаtosis With Polyangiitis Affecting the Lung and Orbit
Вестник рентгенологии и радиологии, 2021 The paper describes a clinical case of pulmonary and right orbital injuries in granulomatosis with polyangiitis in a 38-year-old male. The case is of considerable interest due to the rarity of this pathology, especially because of the localization in the
Zh. V. Sheikh +3 more
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Atypical painless vision loss in a patient with granulomatosis with polyangiitis
, 2020 Vasculitis is a common cause of vision loss, and typically painful. In giant cell arteritis, the most common primary vasculitis in adults, we see elevated inflammatory markers, granulomatous inflammation, and associated headache or scalp tenderness ...
Prospero Ponce, C, Nelson, PC, Kunam, V
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International Forum of Allergy &Rhinology, EarlyView.ABSTRACT Background Chronic rhinosinusitis with nasal polyp (CRSwNP) is a heterogeneous Type 2 inflammatory disease characterized by enhanced eosinophilic infiltration. Both innate and adaptive immunity are involved in the onset and progression of CRSwNP.
Yuki Sonoda +4 more
wiley +1 more source
Granulomatosis with polyangiitis mimicking multisystem pyoderma gangrenosum: A case report
SAGE Open Medical Case ReportsGranulomatosis with polyangiitis, a type of small-medium vessel vasculitis, can pose diagnostic challenges due to its diverse clinical manifestations.
Amanda Gormley, Peter Green
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International Forum of Allergy &Rhinology, EarlyView.ABSTRACT Background Biologic treatments were introduced for chronic rhinosinusitis with nasal polyps (CRSwNP) in 2019. Treatment algorithms for medically refractory CRSwNP remain open, with patients choosing among surgery, biologics, or both. Real‐world utilization of surgery and biologics remains incompletely characterized.
Stephanie Shintani Smith +5 more
wiley +1 more source
SAGE Open Medical Case ReportsGranulomatosis with polyangiitis is a rare autoimmune disorder. Granulomatosis with polyangiitis’s signs and symptoms reflect affected organs, which are inclined toward the respiratory tract and kidneys.
Mohsen Jari +2 more
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Journal of Cardiothoracic Surgery, 2018 Objectives To investigate the risk factors and treatment strategies for pneumothorax secondary to granulomatosis with polyangiitis (GPA). Method Retrospective analysis of cases with pneumothorax secondary to GPA from our own practice and published on ...
Xuhua Shi, Yongfeng Zhang, Yuewu Lu
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Granulomatosis with polyangiitis in Poland – epidemiological study
, 2014 Aim of the study: Granulomatosis with polyangiitis (GPA) is a disease of unknown aetiology, with a variable course, and with the possibility of exacerbations associated with life-threatening organ damage.
Piotr Tyszko +3 more
core +1 more source
Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis [PDF]
, 2017 Eosinophilic granulomatosis with polyangiitis is an eosinophilic vasculitis. Mepolizumab, an anti-interleukin-5 monoclonal antibody, reduces blood eosinophil counts and may have value in the treatment of eosinophilic granulomatosis with ...
José Hernández-Rodríguez +110 more
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