1/9 Let’s talk about nephrotic syndrome after hematopoietic stem cell transplant (HSCT) #Tweetorial #MedTwitter @NSMCInternship

75M with myelofibrosis s/p allogeneic stem cell transplant is referred for nephrotic-range proteinuria discovered during lower extremity edema work up
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Labs show Cr 0.9, albumin 2.0, 24hr urine protein 12g, no RBCs in urine and unremarkable serologic work-up. You decide to pursue a biopsy.

What is the most likely pathologic finding you will find on kidney biopsy?
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Read on to find the answer!

Nephrotic syndrome post-allogeneic HSCT was first described in 1988
💥 Occurs in 0.4-6.0% of pts at a median of ~20 months
💥 Is associated with increased risk of non-relapse related mortality
(Beyar-Katz et al. Biol Blood Marrow Transplant. 2016)
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Nephrotic syndrome post-HSCT is more likely to occur in patients who receive:
🩸 A peripheral blood SCT (thought to be related to ⬆️ T-cell load)
💉 Myeloablative conditioning (thought to be ⬆️ toxic to podocytes)
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Nephrotic syndrome post-HSCT is associated with graft-versus-host disease (GVHD).

💥 Many experts think of Nephrotic syndrome post-HSCT as “kidney GVHD” 👇
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Many case series have shown that the most common pathologic findings on kidney biopsy are:
#1: Membranous nephropathy (~65%)
#2: Minimal change disease (~20%)
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Depending on the histopathologic findings, treatment options include:
👉 Corticosteroids (Cs)
👉 Calcineurin inhibitors (CNIs)
👉 Rituximab

This is mostly based on case reports and case series (see proposed treatment algorithm 👇)
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So let’s try this again. What is the most likely pathologic finding on kidney biopsy in patients with nephrotic syndrome post-HSCT?
Thank you everyone for reading! Here are some pretty photos of membranous nephropathy.

💥 Look out for my next #Tweetorial! #OncoNephrology #MedEd #FOAMed #NSMC
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