Renal Pathology Society
@Renalpathsoc
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Twitter account of the Renal Pathology Society (RPS) #renalpath
Joined January 2018
@Nefrologialapaz La NTIA sigue siendo una patología frecuente. En este artículo revisamos aspectos diagnósticos y terapéuticos prácticos. https://t.co/2rxWeGmMXK
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Onconephrology is a growing subspecialty and important to consider cancer and cancer treatment impacts in evaluation of glomerular disorders. A simplified overview. #GlomerularDiseasesWorkshop
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Antiphospholipid syndrome can cause renal thrombotic microangiopathy. The lesion is not specific and needs positive phospholipid ab test for diagnosis of aPL nephropathy. Picture shows recanalization of occluded interlobular artery in a pt with aPLN
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You can never get bored of listening to @NephRodby @TWhittier_RUSH @Proximal_Baxi @Rush_Nephrology #RushRenalRules @BajinderR @zainabo87 thanks for today’s case 💫
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Case report: De novo C3 Glomerulonephritis in a Kidney Transplant Recipient Associated with an Unreported CFH Variant @KIReports
#openaccess
#C3GN
https://t.co/5BXgbXF0pV
kireports.org
C3 glomerulopathy (C3G), encompassing dense deposit disease (DDD) and C3 glomerulonephritis (C3GN), is defined by predominant C3 deposition in glomeruli without significant immunoglobulin, reflecting...
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Antiphospholipid Syndrome and the Kidney - Kidney International Reports
kireports.org
Antiphospholipid syndrome is a rare autoimmune disorder characterized by the persistent positivity of antiphospholipid antibodies along with thrombotic manifestations, obstetrical complications or...
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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
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Dr @MPAlexanderMD presenting Clonal Monocytosis of Renal Significance @MayoClinicNeph
@onconephsociety
@Renalpathsoc
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Clonal monocytosis and its repercussion on the kidneys @onconephsociety @MayoClinicME @HerrmannMd @LeticiaRolonMD
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In The Literature by @thebeanqueen15 @RichardJJohns11: Native American Ancestry and Susceptibility to Mesoamerican Nephropathy https://t.co/pVbJSe2mWk (FREE)
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Prolidase deficiency (PD) is an autosomal recessive disease resulting in defective collagen synthesis. Patients sometime have overlapping SLE. The case report describes a young woman with PD who has full house GN but with IgA dominance.
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Lupus nephritis case with prominent podocyte cytoplasmic vacuolization on LM with myelin figures revealed by EM. Probably HCQ effect but given its prominence genetic etiologies should be excluded (e.g., Fabry, LMX1B). #renalpath #pathtwitter #nephrology
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This one is a classic. Large well demarcated granulomas with giant cells. Dx: Granulomatous interstitial nephritis, associated with Sarcoidosis. Differential diagnosis includes drug-induced interstitial nephritis. 60 yr-old with HTN, sarcoidosis & rise in Cr from 1.1 to 2.5.
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Tubular atrophy in endocrine pattern. The tubules are small with cuboidal epithelium and narrow lumens. TBM is thin and delicate. This pattern of tubular atrophy has been associated with stenosis of renal artery and its major branch.
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A special thanks to @AngelottiLucia, our microscopy expert. With her talent, even the toughest forms of high-resolution imaging becomes easy. She brings essential contributions, and a touch of beauty to all our studies 🔬💡 https://t.co/P2ATMuUCa6
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Difficult case. Needed my thinking cap LM=Necrotizing & crescentic glomerulonephritis Few crescents~Napoleon’s cap IF=3+ IgG & C3 in crescents & 2+ in mesangium & capillary walls EM=subendo+mesangial deposits Dx-Crescentic GN, likely infection-related (endocarditis/clinical)
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