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Tracheobronchial amyloidosis: a bright sight with autofluorescence light

T De Keukeleire1, S Hanon, B Dieriks

  • 1Interventional Endoscopy Clinic and Respiratory Division, Academisch Ziekenhuis, Vrije Universiteit Brussels, Brussels, Belgium. tom.dekeukeleire@az.vub.ac.be

Respiration; International Review of Thoracic Diseases
|January 24, 2007
PubMed
Abstract

No abstract available in PubMed .

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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...