@grace_choung Important update to this! Trichrome staining in fibronectin glomerulopathy turns out to be highly variable. See the tweet by @SethiRenalPath
@grace_choung One peculiar feature of fibronectin glomerulopathy: it’s the only glomerular deposition disorder with red deposits on trichrome stain — a distinctive clue. #renalpath#PathTwitter
This was a difficult but good teaching case.
Easy to call idiopathic MPGN but…
LM: Membranoproliferative Glomerulonephritis (MPGN) pattern
IF- dull minimal IgG IgM C3 kappa lambda
EM- massive deposits.
Pronase IF/IgG subclass all negative. At this point I had an idea-
FIBRONECTIN GLOMERULOPATHY
Did mass spectrometry. Confirmed the diagnosis=Large amounts of fibronectin.
55 yr old with proteinuria and declining renal function.
@SethiRenalPath Excellent teaching case Sir. Could you please share the Masson trichrome stain for this case ? I have always felt that fibronectin glomerulopathy is perhaps the only glomerular deposition disease showing characteristic red deposits on Masson trichrome. Would you agree?
Multiple diagnoses not uncommon in kidney biopsies. This case showed nodular diabetic nephropathy, a mostly chronic ANCA associated GN, and to top it off some interstitial ALECT2 amyloidosis. #renalpath#nephrology#PathTwitter
The Renal Pathology Society warmly invites nephropathologists and non-pathologists involved in the interpretation of kidney biopsies to participate in a global survey.
More info. below 👇
https://t.co/BIIDgPid6u
@GlomCon@ISNkidneycare#renalpath
@JerasitS@grace_choung Thank you for sharing this striking image, Jerasit. Perhaps fibronectin glomerulopathy should be considered in the differential whenever red deposits are seen on Trichrome in glomerular deposition disorders. #renalpath@JZRenalPath@vinaypush@RitambhraN
@kiddo_kidney@Renalpathsoc@draalok@RitambhraN@vinaypush@JZRenalPath Protein reabsorption droplets are mainly (pink) granular rather than vacuolar. These droplets are highlighted by PAS stain and are commonly identified in Nephrotic syndrome.
Will try to share some pics soon.
Capillary wall "eye-lashes" not always amyloid. Rare finding in a recent fibrillary case. IF = IgG. IHC = DNJAB9. Congo red (-). #renalpath#pathtwitter
Older patient with anasarca. Bx with massive glomerular amyloidosis - AH type. IF and EM reveal concurrent heavy chain deposition disease. Unusual dual diagnosis. #renalpath#nephrology#pathtwitter
AKi in a pt with recent contrast administration and antibiotic use. Features of contrast nephropathy and allergic interstitial nephritis. #renalpath#pathtwitter
@draalok@RitambhraN@vinaypush@JZRenalPath@Renalpathsoc Before making a diagnosis of acute CNI toxicity with Tubular foam cells, we need to think of:
1. Ischemic acute tubular injury
2. Osmotic tubulopathy
3. Potassium depletion
4. Nephrotic syndrome
A reminder that cryoglobulinemic glomerulonephritis can still occur post-HCV treatment. Biopsy for hematuria, proteinuria, and elevated sCr. Low c3/c4. +cryocrit and RF. #renalpath#pathtwitter