Results 41 to 50 of about 11,205 (172)
Rapidly progressive (crescentric) glomerulonephritis in erythema nodosum leprosum: case report
Hansenologia Internationalis, 1986 A middle aged man (48 years) with short duration of illness (7 days) was admitted in the state of acute renal failure with erythema nodosum leprosum. He had repeated episodes of erythema nodosum leprosum in the past.
Pranesh Pranesh NIGAM +7 more
doaj +1 more source
Microscopic polyangiitis hiding behind the mask of COVID-19: A case series and minireview
Український Журнал Нефрології та Діалізу, 2023 Microscopic polyangiitis (MPA) is one of the three clinical phenotypes of vasculitis associated with antineutrophil cytoplasmic antibodies (ANCA). Although MPA is considered a rare form of ANCA-associated vasculitis (AAV), clinical evidence shows that ...
Tetyana I. Yarmola +5 more
doaj +1 more source
Alimentary Pharmacology &Therapeutics, Volume 63, Issue 7, Page 945-954, April 2026.Current first‐line NUCs show comparable renal safety profiles in CHB patients with no or mild kidney dysfunction, with growing evidence that favours TAF. Future prospective studies are needed to validate these findings, and more research should focus on CHB patients with diabetes mellitus who are at risk of CKD.
Lung‐Yi Mak +2 more
wiley +1 more source
Rapidly progressive glomerulonephritis: A wild card manifestation of lupus nephritis
Saudi Journal of Kidney Diseases and Transplantation, 2018 A significant proportion of individuals with systemic lupus erythematosus (SLE) will have clinical or laboratory evidence of renal involvement at some point in the course of their disease.
Opeyemi O Komolafe
doaj +1 more source
Indian Journal of Pathology and Microbiology, 2020 Various renal abnormalities in leprosy have been described largely in literature but the occurrence of IgA dominant infection related glomerulonephritis in leprosy with type 2 lepra reaction has not been reported so far. We present here a 60-year-old man
Elayaperumal Indhumathi +4 more
doaj +1 more source
Immunology, Volume 177, Issue 4, Page 736-748, April 2026.A constant rate of DNA damage that is not perfectly repaired will cause a constant rate of DNA mutations. The chance of mutation will increase if DNA is prone to damage, such as occurs in somatic hypermutation (SHM) hotspots and GC‐rich DNA. Thus, if one mutation‐prone DNA site drives disease, the age of onset of disease and degree of penetrance should
Piet C. de Groen
wiley +1 more source
Saudi Journal of Kidney Diseases and Transplantation, 2018 We describe here a case of a 53-year-old Saudi female who presented to the emergency room with shortness of breath progressive in nature for the previous one month, associated with a cough and occasional greenish sputum.
Ahmad Alflaiw +3 more
doaj +1 more source
Advanced Science, Volume 13, Issue 14, 9 March 2026.This review outlines association between vasculitis and malignancies and provides practical value for clinicians in distinguishing primary vasculitis from malignancy‐associated forms and optimizing patient surveillance, improving recognition of tumor‐associated vasculitis to reduce the risk of misdiagnosis, supporting more accurate clinical decision ...
Xiaofei Shi +8 more
wiley +1 more source
Arthritis &Rheumatology, Volume 78, Issue 3, Page 695-704, March 2026.Objective The phase 3 MANDARA study demonstrated noninferiority of benralizumab versus mepolizumab for remission in patients with eosinophilic granulomatosis with polyangiitis (EGPA). More benralizumab‐treated patients achieved complete withdrawal of oral glucocorticoids (OGCs).
Parameswaran K. Nair +14 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Granulomatosis with polyangiitis can rarely present as deep vein thrombosis in adolescents. Unexplained thrombosis in a young patient, accompanied by systemic inflammatory features, should raise suspicion for an underlying vasculitis. Early recognition and prompt initiation of immunosuppressive therapy alongside anticoagulation are crucial to ...
Bishal Budha +8 more
wiley +1 more source