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Views on study design for lupus nephritis research
You can read more about the research in our article here: https://lupusuk.org.uk/views-on-study-design-for-lupus-nephritis-research/
Or jump straight to the survey here: https://app.onlinesurveys.jisc.ac.uk/s/bham/inflammatory-glomerulonephritis
A questionnaire for those with ANCA associated vasculitis and renal involvement in the UK
https://app.onlinesurveys.jisc.ac.uk/s/bham/inflammatory-glomerulonephritis
Can you please take 3 minutes to answer the questions?
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Macrophages, type of immune cell, tied to lupus nephritis in children
More M1-like macrophages and B-cells linked to poorer kidney function
Children with other kidney diseases included 15 with post-infectious glomerulonephritis, 11 with hemolytic uremic syndrome, 11 with membranoproliferative glomerulonephritis, and nine with ANCA-associated pauci-immune glomerulonephritis
Autoimmune hemolytic anemia (AIHA), Immune thrombocytopenia (ITP) and other autoimmune complications and extranodal involvement in CLL
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[u]Acquired von Willebrand disease[/u] and [u]acquired hemophilia A[/u]
Non-hematologic autoimmune conditions: [u]Paraneoplastic pemphigus[/u], [u]Glomerulonephritis[/u], [u]Angioedema due to acquired C1 esterase inhibitor deficiency[/u] ("[i]C1 esterase inhibitor deficiency has been reported
Dual diagnosis of histiocytoid Sweet syndrome and anti-neutrophil cytoplasmic antibody-associated vasculitis
"Our patient had a very rare combination of H-SS skin lesions in the setting of ANCA proteinase-3 granulomatosis with polyangiitis glomerulonephritis."
ADDITIONAL NOTE.
HISTIOCYTOID SWEET'S SYNDROME: In Sweet’s syndrome, mature white blood cells called neutrophils accumulate in the tissues.