AJKD Atlas of Renal Pathology: Fibronectin Glomerulopathy - PubMed
AJKD Atlas of Renal Pathology: Fibronectin Glomerulopathy
πΈMostly adults
πΈProteinuria/hematuria
πΈESRD 10-20 yrs
πΈNo specific treatment
References:
pubmed.ncbi.nlm.nih.gov/29055354/
(2/2)
06.08.2025 03:18 β π 1 π 2 π¬ 1 π 0
H&E showing glomerulus with MPGN-like pattern
Immunofluorescence strongly staining for fibronectin
Electron microscopy - homogeneous granular electron dense deposits
Fibronectin glomerulopathy
πΈMassive fibronectin deposits
πΈAD mutation FN1
πΈMPGN-like pattern
πΈSilver-neg, PAS+, trichrome-red
πΈEM: Homogeneous granular + variable fibrils
πΈIF/IHC strongly + fibronectin
πΈrenal-limited
(1/2) more below
#renalpath #pathsky #nephsky
06.08.2025 03:18 β π 6 π 4 π¬ 1 π 0
#RenalPath: Lecithinβcholesterol acyltransferase deficiency with mild mesangial expansion with slight foamy appearance. Capillary walls show segmental thickening (hematoxylin and eosin stain).
bit.ly/2tQDkJx (FREE)
13.04.2025 10:01 β π 8 π 4 π¬ 0 π 0
Excuse the βtaking a picture of a computer screenβ quality here - this looks like early MN pattern (IgG, IgG1 here) by IF, but EM has absolutely no deposits (EM on frozen material done on this glom). Still MN (βby IF onlyβ?!)? @glombandit.bsky.social @arkanalabs.bsky.social @jzrenalpath.bsky.social
09.08.2025 17:03 β π 5 π 3 π¬ 4 π 0
16.07.2025 20:15 β π 0 π 0 π¬ 0 π 0
AVF dysfunction due to partial thrombosis at the anastomosis. Previous gradual anastomotic thrombosis led to peripheral blood flow and arteriopoesis with aneurysmatous dilation of cannulation site, which is now collapsing at blood flow rates higher then 200ml/min.
16.07.2025 20:10 β π 1 π 0 π¬ 1 π 0
Pt has DM, heavy proteinuria & CKD. Bx shows fx of nodular diabetic GS. BUT EM also shows large substructures. IF with strong fibrinogen in similar glomerular distribution as substructures. Other than linear weak IgG & albumin, Ig's & LC's (-). What could they be?
#renalpath #pathsky #nephsky
05.04.2025 03:44 β π 4 π 6 π¬ 3 π 0
Diabetic fibrillosis?
16.07.2025 19:52 β π 1 π 0 π¬ 1 π 0
#RenalPath: Postinfectious glomerulonephritis with irregular, coarse granular capillary loop and mesangial staining for immunoglobulin G (immunofluorescence microscopy).
bit.ly/2KwRGU4 (FREE)
06.04.2025 10:00 β π 4 π 4 π¬ 0 π 0
My patients live at the margins of society. They donβt have much. Just getting to dialysis three times a week is a big ask. Taking from them to fund tax breaks for the rich is just cruel.
I want to be outraged but I just feel like crying.
02.07.2025 00:20 β π 64 π 24 π¬ 2 π 0
Strong linear IgG involving proximal tubular basement membranes
Acute tubular injury
Chronic tubulointerstitial nephritis (trichrome stain)
Electron microscopy shows atrophic tubular basement membranes. No deposits are seen.
Anti-tubular basement membrane (TBM) disease
πΈRare type of tubulointerstitial nephritis
πΈStrong linear polyclonal IgG restricted to TBMs
πΈNo deposits by EM
πΈAutoantibody to TIN-ag in proximal TBM
πΈAKI/CKD, polyuria, polydipsia
Reference: ajkd.org/article/s027...
#renalpath #pathsky #nephsky
03.07.2025 04:00 β π 6 π 3 π¬ 1 π 0
In late March, the FDA approved iptacopan to reduce proteinuria in patients with C3 glomerulopathy. With additional approvals anticipated to treat this rare condition, education on identifying and treating C3G is critical. kidney.pub/KN1706-02
#ASNKidneyNews
03.07.2025 15:00 β π 4 π 3 π¬ 0 π 0
#RenalPath: CNI nephrotoxicity with TMA involving an arteriole (Jones silver stain).
bit.ly/2qeBWhV (FREE)
22.06.2025 10:01 β π 8 π 4 π¬ 0 π 0
#RenalPath: Nail-patellaβlike renal disease (also known as LMX1B-associated nephropathy) with segmental glomerulosclerosis in a 39-year-old man with dystrophic nails, but no patellar or other skeletal abnormalities (Jones silver stain).
https://bit.ly/42h16yf (FREE)
02.02.2025 11:00 β π 9 π 3 π¬ 0 π 0
Muddy brown granular cast and fragmented renal tubular epithelial cell cast under interference contrast illumination. Case of ATN, AKI. #UrinarySediment #UrineMicroscopy #PisseProphet #renalpath
16.01.2021 21:35 β π 3 π 2 π¬ 0 π 0
Pediatric anti-phospholipid syndrome (APS) is a rare autoimmune inflammatory disorder resulting in recurrent vascular thrombosis w/serious clinical implications. Read these Clinical Insights into pediatric APS nephropathy.
link.springer.com/article/10.1...
03.07.2025 17:09 β π 4 π 4 π¬ 0 π 0
Genetic testing is crucial in nephrology, as up to 10% of kidney disease patients receive a genetic diagnosis. This review aims to explain the genetic counseling process and relevance to patients, enabling comprehensive care for their genetic and clinical needs. kidney.pub/KID0825
#ASNKidney360
21.06.2025 17:29 β π 9 π 5 π¬ 1 π 0