Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 23, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Differential Diagnosis for Membranous Glomerulonephritis

Single Most Likely Diagnosis

  • Primary Membranous Nephropathy: This is the most common cause of membranous glomerulonephritis in adults, characterized by the presence of subepithelial immune complex deposits. The high proteinuria (88) and significant albumin-to-creatinine ratio (ACR of 55) support this diagnosis, as primary membranous nephropathy often presents with nephrotic syndrome.

Other Likely Diagnoses

  • Secondary Membranous Nephropathy due to Autoimmune Diseases: Conditions like systemic lupus erythematosus (SLE) can cause membranous glomerulonephritis. The presence of high proteinuria and significant ACR could be indicative of an underlying autoimmune process.
  • Secondary Membranous Nephropathy due to Infections: Certain infections, such as hepatitis B, can lead to membranous glomerulonephritis. The clinical context and additional testing would be necessary to consider this diagnosis.
  • Secondary Membranous Nephropathy due to Medications: Some medications are known to cause membranous nephropathy, including non-steroidal anti-inflammatory drugs (NSAIDs) and certain antibiotics. A thorough medication history is essential.

Do Not Miss Diagnoses

  • Diabetic Nephropathy: Although the primary presentation is different, diabetic nephropathy can sometimes present with significant proteinuria and could be considered, especially in patients with long-standing diabetes. Missing this diagnosis could lead to inadequate management of diabetes and its complications.
  • Amyloidosis: This condition can cause nephrotic syndrome and should be considered, especially if there are other systemic symptoms or if the patient has a history of chronic diseases that could lead to amyloid deposition.

Rare Diagnoses

  • Alport Syndrome: A genetic disorder affecting the type IV collagen in the glomerular basement membrane, leading to chronic kidney disease and sometimes presenting with significant proteinuria. However, it typically has a different clinical presentation and is less likely.
  • Membranoproliferative Glomerulonephritis: A type of glomerulonephritis that can present with both nephritic and nephrotic features. It is less common and the clinical and histological findings would need to align closely with this diagnosis.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.