[A case of primary amyloidosis associated with giant cell infiltration within a Bowman's capsule]

K Song-su1, T Mitarai, H Tamura

  • 1Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School.

Insights

This study reports a rare case of primary amyloidosis in a 67-year-old man with nephrotic syndrome. Giant cell infiltration in the kidney

Area of Science:

  • Nephrology
  • Pathology
  • Immunology

Background:

  • Nephrotic syndrome is a kidney disorder characterized by heavy protein loss in urine.
  • Primary amyloidosis involves abnormal protein deposits in organs, often affecting the kidneys.
  • Monoclonal gammopathy indicates abnormal protein production by plasma cells.

Observation:

  • A 67-year-old male presented with nephrotic syndrome, generalized edema, and macroglossia.
  • Kidney biopsy revealed amyloid deposits in glomeruli and interstitial cell infiltration, including multinucleated giant cells.
  • Amyloid deposits were confirmed via Congo red staining and electron microscopy, and found in other tissues.

Findings:

  • The patient exhibited IgA lambda monoclonal gammopathy, indicative of lambda light chain amyloidosis.
  • Amyloid deposits were resistant to potassium permanganate, a characteristic of certain amyloid types.
  • Multinucleated giant cell infiltration in Bowman's capsule is a novel finding in primary amyloidosis.

Implications:

  • This case highlights a unique presentation of primary amyloidosis with giant cell infiltration.
  • The findings expand the understanding of the pathological features associated with primary amyloidosis.
  • Further research may elucidate the role of giant cells in the pathogenesis of primary amyloidosis.

Related Concept Videos

Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...
Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...
Alzheimer Disease ll: Pathophysiology01:23

Alzheimer Disease ll: Pathophysiology

Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and microglia. Abnormal...