Pathology · Immunopathology (Hypersensitivity, Autoimmunity, Immunodeficiency, Amyloidosis)

A 65-year-old man with long-standing multiple myeloma develops progressive nephrotic syndrome. Congo red staining of renal biopsy shows apple-green birefringence under polarized light in the mesangium and vessel walls. The amyloid protein in this clinical context is:

  • A AA amyloid (serum amyloid A protein)
  • B ATTR amyloid (transthyretin)
  • C AL amyloid (immunoglobulin light chains)
  • D Aβ2M amyloid (beta-2 microglobulin)
Correct answer: C. AL amyloid (immunoglobulin light chains)

Explanation

Multiple myeloma produces excess immunoglobulin light chains (usually lambda or kappa); these are deposited as AL amyloid (primary amyloidosis) which is the most common systemic amyloidosis in developed countries. AA amyloid derives from serum amyloid A in chronic inflammatory states (reactive amyloidosis). ATTR amyloid is associated with age-related and hereditary cardiac amyloidosis; Aβ2M amyloid occurs in dialysis patients.

Reference: Robbins & Cotran Pathologic Basis of Disease, 10th ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

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