Clinical features and pathogenesis of membranoproliferative glomerulonephritis: a nationwide analysis of the Japan renal biopsy registry from 2007 to 2015 [PDF]
, 2018 BackgroundThe incidence and age distribution of membranoproliferative glomerulonephritis (MPGN) vary throughout the world by race and ethnicity. We sought to evaluate the clinical features, pathogenesis, and age distribution of MPGN among a large ...
Hasebe Naoyuki +11 more
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The pathological diagnosis of nerve biopsies: a practical approach [PDF]
, 2016 The approach to the neuropathological assessment of nerve biopsies is the main focus of this review. Nerve biopsies are invasive diagnostic procedures resulting in a permanent neurological deficit, and are therefore carried out only following an in-depth
Brandner, S
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Palbociclib-induced IgA vasculitis
Dermatology Online Journal, 2022 Patel, Payal M +2 more
openaire +4 more sources
Annular leukocytoclastic vasculitis: a new feature of IgA vasculitis
European Journal of Case Reports in Internal MedicineBackground: Annular erythema is a rare manifestation of leukocytoclastic vasculitis. It may be associated with various drugs, infections, malignancies, or systemic diseases. Case description: A 36-year-old woman with no personal medical history presented with annular erythema with target lesions and petechial purpura.
Nabil Belfeki +5 more
openaire +3 more sources
, 2005 A 30 year old man is referred for a medical check up before taking a life insurance policy. He is asymptomatic, gives no relevant history, is on no treatment and physical examination is unremarkable. Routine dip-stick analysis of a midstream specimen of
Vella, Mario P.
core
Histopathological findings in elderly patients [PDF]
, 2010 INTRODUCTION: The elderly population has significantly increased worldwide and recent studies have evidenced a 10-year increase in Brazilian life expectancy.
Bastos, Marcus Gomes +4 more
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Use of Plasmapheresis and Immunosuppressants to Treat Diffuse Alveolar Hemorrhage in a Patient with Granulomatosis with Polyangiitis. [PDF]
, 2019 Granulomatosis with polyangiitis (GPA) is a systemic granulomatous inflammatory disease characterized by small-to-medium vessel vasculitis due to Central Anti-Neutrophil Cytoplasmic Antibody (C-ANCA).
Sattar, Yasar +4 more
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IgA Vasculitis with Simultaneous Cardiopulmonary Involvement
Internal Medicine, 2018 A 60-year-old man with a history of hypertension, type 2 diabetes, and reflux esophagitis was admitted to our hospital with hemoptysis, dyspnea, and leg edema. We diagnosed him with adult IgA vasculitis based on the presence of purpura, elevated serum IgA fibronectin complexes, pathophysiological findings, a skin biopsy showing leukocytoclastic ...
Bando, Kazunori +2 more
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IgA Vasculitis in a Patient with Type 2 Diabetes Complicated by Severe Diabetic Nephropathy
Clinical DiabetologyWe encountered a case of IgA vasculitis in a patient with type 2 diabetes mellitus and severe renal failure (CKD classification; grade IV). A typical skin rash was seen on both lower extremities, which led us to believe that the patient had IgA ...
Shuichi Okada +5 more
doaj +1 more source
Blistering eruptions with tissue eosinophilia in a child with IgA vasculitis
Clinical Case Reports, 2018 Key Clinical Message We present a child with bullous IgA vasculitis. Because skin biopsy showed epidermal vesicles with neutrophil infiltration and leukocytoclastic vasculitis in all layers of the dermis, with IgA deposits and tissue eosinophilia ...
Toru Watanabe, Shinya Tsukano
doaj +1 more source