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The kidneys are intricate organs with millions of working units known as nephrons. Each nephron features two major structures: the renal corpuscle, which facilitates blood plasma filtration, and the renal tubule, which handles the glomerular filtrate. Blood supply is directly linked to the nephrons. The renal corpuscle consists of the glomerulus, a capillary network, and the Bowman's capsule, a double-walled epithelial structure that encases the glomerulus. The filtering of blood plasma...
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The glomerulus and Bowman's capsule are two essential components of the nephron, which is the functional unit of the kidney. These microscopic structures play a critical role in the process of blood filtration to produce urine.
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Updated: Jun 17, 2025

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Nephrotic Syndrome Without Nephrotic Range Proteinuria.

Jibran A Sheikh1, Usheem Syed1, Sayed M Osama2

  • 1Internal Medicine, Central Michigan University College of Medicine, Saginaw, USA.

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|August 12, 2024
PubMed
Summary
This summary is machine-generated.

Nephrotic syndrome can occur even without the standard 3.5g/24h proteinuria threshold. This case highlights systemic amyloid light chain (AL) amyloidosis causing nephrotic syndrome with lower proteinuria levels due to liver disease.

Keywords:
albumin clearancehepatic amyloidosisnephrotic syndromenephrotic-range proteinuriasystemic amyloidosis

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Area of Science:

  • Nephrology
  • Internal Medicine
  • Hematology

Background:

  • Nephrotic syndrome is typically defined by proteinuria ≥3.5g/24h, low serum albumin, edema, and hyperlipidemia.
  • This definition's arbitrary threshold may not capture all cases with glomerular permeability defects.

Observation:

  • A 57-year-old male presented with severe edema, fatigue, and reduced urine output.
  • Laboratory results showed low serum albumin (1.3 g/dL), moderate proteinuria (2.3g/24h), and hypercholesterolemia.
  • Renal biopsy revealed amyloid light chain (AL) amyloidosis, confirmed by bone marrow biopsy.

Findings:

  • A diagnosis of nephrotic syndrome secondary to systemic AL amyloidosis was established, despite proteinuria below the 3.5g/24h threshold.
  • Concurrent hepatic amyloidosis was identified through various imaging and laboratory tests.
  • Reduced albumin synthesis due to liver disease can lead to nephrotic syndrome at lower proteinuria levels.

Implications:

  • This case challenges the rigid diagnostic criteria for nephrotic syndrome.
  • It underscores the importance of considering systemic diseases like AL amyloidosis in atypical presentations.
  • Accurate diagnosis is crucial for timely and appropriate management of nephrotic syndrome and its underlying causes.