Local deposition of amyloid without systemic involvement is rather uncommon and has been found in many organs. A 67-year-old man was admitted to our hospital presenting with weight loss, fatigue and poor appetite. Blood work and bone marrow examination revealed megaloblastic anemia. Upper gastrointestinal endoscopy reveeled e purple polypoid wass lesion of 5mm eliameter in the paracardiac region. Histopathologic examination of the gastric biopsy showed the deposition of amyloid materials in the mucosa. The patient had no evidence suggesting systemic amyloidosis. We report a rare case of localized amyloidosis of the stomach. The clinical and pathological features of this rare condition and association with megaloblastic anemia are discussed
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
primary amyloidosis is a rare disrder wihich is diagnosed by extracellular deposition of proteinaceo...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
Abstract Introduction Amyloidosis most often manifests as a systemic involvement of multiple tissues...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Esophagogastroduodenoscopy for cancer screening was performed in a 55-year-old woman as part of a he...
Amyloid may cause widespread damage to the gastrointestinal tract. Affection of blood vessels may le...
Amyloidosis of the gastrointestinal tract is usually a systemic disease. Localized gastrointestinal ...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
An unusual case of amyloid deposition in the wall of gastric pouch 15 years after surgery for peptic...
Poster no. C-1406Amyloidosis is an uncommon heterogeneous group of diseases caused by extracellular ...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
© 2018 S. Karger AG, Basel. Copyright: All rights reserved. Objective: Amyloidomas are tumor-like de...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
primary amyloidosis is a rare disrder wihich is diagnosed by extracellular deposition of proteinaceo...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
Abstract Introduction Amyloidosis most often manifests as a systemic involvement of multiple tissues...
A 65-year-old Hispanic female presented with a one-year history of anorexia, nausea, early satiety, ...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Esophagogastroduodenoscopy for cancer screening was performed in a 55-year-old woman as part of a he...
Amyloid may cause widespread damage to the gastrointestinal tract. Affection of blood vessels may le...
Amyloidosis of the gastrointestinal tract is usually a systemic disease. Localized gastrointestinal ...
Amyloidosis is a rare disease caused by extracellular deposits of insoluble fibrillar proteins in va...
An unusual case of amyloid deposition in the wall of gastric pouch 15 years after surgery for peptic...
Poster no. C-1406Amyloidosis is an uncommon heterogeneous group of diseases caused by extracellular ...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
© 2018 S. Karger AG, Basel. Copyright: All rights reserved. Objective: Amyloidomas are tumor-like de...
Amyloidosis is characterized by the accumulation of an insoluble amyloid protein in the extracellula...
primary amyloidosis is a rare disrder wihich is diagnosed by extracellular deposition of proteinaceo...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...