Poster no. C-1406Amyloidosis is an uncommon heterogeneous group of diseases caused by extracellular deposition of the amyloid protein. The amyloid deposits demonstrate apple-green birefringence under a polarized light microscope after staining with Congo red, and presence of rigid and non-branching fibrils of 7.5-10 nm diameters on electron microscopy. Amyloidosis can be classified into systemic or localized forms. The gastrointestinal tract (GIT) is the commonest site of involvement (98%) of systemic...link_to_OA_fulltex
absence of any other disease, as well as a review of relevant literature. CASE REPORT A 62-year-old ...
Amyloidosis is a rare hereditary or acquired protein deposition disorder with different etiologies, ...
Local deposition of amyloid without systemic involvement is rather uncommon and has been found in ma...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Amyloid may cause widespread damage to the gastrointestinal tract. Affection of blood vessels may le...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
The involvement of the small bowel in systemic forms of amyloidosis may be diffuse or very rarely fo...
Introduction: The systemic amyloidosis usually doesn’t save the digestive tract, but this involvemen...
Amyloidosis is a pathologic diagnosis characterized by extracellular deposition of insoluble protein...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
Gastrointestinal (GI) amyloidosis represents a significant diagnostic challenge due to its nonspecif...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
Introduction. Amyloidosis is a rare disease associated with extracellular accumulation of abnormal p...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
absence of any other disease, as well as a review of relevant literature. CASE REPORT A 62-year-old ...
Amyloidosis is a rare hereditary or acquired protein deposition disorder with different etiologies, ...
Local deposition of amyloid without systemic involvement is rather uncommon and has been found in ma...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Amyloid may cause widespread damage to the gastrointestinal tract. Affection of blood vessels may le...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
The involvement of the small bowel in systemic forms of amyloidosis may be diffuse or very rarely fo...
Introduction: The systemic amyloidosis usually doesn’t save the digestive tract, but this involvemen...
Amyloidosis is a pathologic diagnosis characterized by extracellular deposition of insoluble protein...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
Gastrointestinal (GI) amyloidosis represents a significant diagnostic challenge due to its nonspecif...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
Introduction. Amyloidosis is a rare disease associated with extracellular accumulation of abnormal p...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
absence of any other disease, as well as a review of relevant literature. CASE REPORT A 62-year-old ...
Amyloidosis is a rare hereditary or acquired protein deposition disorder with different etiologies, ...
Local deposition of amyloid without systemic involvement is rather uncommon and has been found in ma...