Abstract Introduction Amyloidosis most often manifests as a systemic involvement of multiple tissues and organs, and an amyloidal deposit confined to the stomach is extremely rare. It is sometimes difficult to provide a definitive diagnosis of localized gastric amyloidosis by biopsy specimen and diagnosis of amyloidosis in some cases has been finalized only after surgical resection of the stomach. Case presentation A 76-year-old Japanese woman with epigastric discomfort underwent an esophagogastroduodenoscopy procedure. The esophagogastroduodenoscopy revealed gastric wall thickening, suggesting scirrhous gastric carcinoma, at the greater curvature from the upper to the lower part of the gastric corpus. A biopsy specimen revealed amyloid dep...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Introduction . Primary amyloidosis is a disorder resulting from the deposition of fibrillary protein...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
Local deposition of amyloid without systemic involvement is rather uncommon and has been found in ma...
Esophagogastroduodenoscopy for cancer screening was performed in a 55-year-old woman as part of a he...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
© 2018 S. Karger AG, Basel. Copyright: All rights reserved. Objective: Amyloidomas are tumor-like de...
An unusual case of amyloid deposition in the wall of gastric pouch 15 years after surgery for peptic...
Upper gastrointestinal endoscopy was performed in patients with rheumatoid arthritis (RA) during the...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
http://dx.doi.org/10.1136/bcr.01.2011.3775 AuthorAmyloidosis occurs as a result of the extracellula...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Poster no. C-1406Amyloidosis is an uncommon heterogeneous group of diseases caused by extracellular ...
Amyloidosis is a pathologic diagnosis characterized by extracellular deposition of insoluble protein...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Introduction . Primary amyloidosis is a disorder resulting from the deposition of fibrillary protein...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
Local deposition of amyloid without systemic involvement is rather uncommon and has been found in ma...
Esophagogastroduodenoscopy for cancer screening was performed in a 55-year-old woman as part of a he...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
© 2018 S. Karger AG, Basel. Copyright: All rights reserved. Objective: Amyloidomas are tumor-like de...
An unusual case of amyloid deposition in the wall of gastric pouch 15 years after surgery for peptic...
Upper gastrointestinal endoscopy was performed in patients with rheumatoid arthritis (RA) during the...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
http://dx.doi.org/10.1136/bcr.01.2011.3775 AuthorAmyloidosis occurs as a result of the extracellula...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
Poster no. C-1406Amyloidosis is an uncommon heterogeneous group of diseases caused by extracellular ...
Amyloidosis is a pathologic diagnosis characterized by extracellular deposition of insoluble protein...
Amyloidosis is a disease marked by deposition of misfolded proteins, known as amyloids, in the extra...
Introduction . Primary amyloidosis is a disorder resulting from the deposition of fibrillary protein...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...