Results 81 to 90 of about 6,839 (215)
A case of myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated glomerulonephritis and concurrent membranous nephropathy [PDF]
BACKGROUND: Myeloperoxidase anti-neutrophil cytoplasmic antibody-associated glomerulonephritis (MPO-ANCA-GN) and concurrent membranous nephropathy (MN) are very rare combination. Their causal relationship has been suggested, but not determined.
Hideaki Yamabe +8 more
core +1 more source
Introduction Pheochromocytomas are rare catecholamine‐producing neuroendocrine tumors that present with the classical triad of paroxysmal hypertension, palpitations, and sweating; however, this presentation is seen in less than 1/4 of pheochromocytoma patients. Hypertension is usually the predominant manifestation.
Anum Rizwan +7 more
wiley +1 more source
Current concepts in C3 glomerulopathy
Complement component 3 glomerulopathy (C3G) is a recently defined entity comprising of dense deposit disease and C3 glomerulonephritis. The key histological feature is the presence of isolated C3 deposits without immunoglobulins. Often masqueradng as some of the common glomerulonephritides this is a prototype disorder occurring from dysregulated ...
Thomas, S. +4 more
openaire +2 more sources
Immunoglobulin A Nephropathy and Malaria falciparum Infection; a Rare Association [PDF]
Glomerular involvement occurs as a rare form of renal manifestation in Plasmodium falciparum malaria. Here, we report a rare case of falciparum malaria-associated IgA nephropathy.
Alizadeh, Farshid. +4 more
core +2 more sources
Introduction The heterogeneity of membranous nephropathy is well described in the literature, and its clinical course and response to treatment vary. Similarly, acute interstitial nephritis (AIN) can present in unexpected and unusual ways and should always be considered within the differential diagnosis of worsening renal function.
Jarrad Hopkins +4 more
wiley +1 more source
Four cases of C3 glomerulopathy in children and literature review [PDF]
Objective To investigate the clinical phenotypes, pathological characteristics, genetic variants, and treatment outcomes in children with C3 glomerulopathy (C3G), and to provide evidence for precise diagnosis and management.
LI Huarong, CHEN Chaoying, TU Juan, LIN Tiantian, WANG Nannan
doaj +1 more source
Intersecting Autoimmunities: ANCA and Anti‐GBM Overlap in a Patient With Sjögren’s Disease
Background The coexistence of antineutrophil cytoplasmic antibodies (ANCAs) and antiglomerular basement membrane (anti‐GBM) antibodies defines a rare but clinically significant autoimmune overlap syndrome. This dual positivity can result in rapidly progressive glomerulonephritis, often with poor kidney outcomes. Diagnosis is particularly challenging in
Mayra Estacio +4 more
wiley +1 more source
Renal transplant pathology: main morphological findings and how to sign out biopsies [PDF]
Renal transplant has reached remarkable and growing rates of success since its introduction; nowadays it is a widely used replacement therapy. Renal allograft biopsies are increasingly more frequent in the routine of pathology laboratories, whose ...
Araújo, Sérgio +9 more
core +2 more sources
Purpose This systematic review aims to synthesize data from biopsy‐based studies to quantify the epidemiology, regional variations, and temporal trends of glomerular diseases (GDs) in Saudi Arabia. Methods We conducted a systematic search using PubMed, MEDLINE, the Cochrane Library, and Google Scholar to identify relevant studies published up to ...
Manal E. Alotaibi +6 more
wiley +1 more source
ABSTRACT Lupus nephritis (LN) is one of the most severe manifestation of systemic lupus erythematosus (SLE). However, reliable tools for predicting LN risk remain limited. In this multicenter prospective cohort study, we developed, validated, and refined a risk stratification model for new‐onset LN.
Yufang Ding +24 more
wiley +1 more source

