A 48-year-old female with multiple myeloma (MM) and amyloidosis presented with massive upper gastrointestinal (GI) bleeding one week after autologous stem cell transplantation (autologous-SCT). Esophagogastroduodenoscopy (EGD) demonstrated necrotic, purple, pigmented, friable lesions throughout the stomach (Figure 1a), along with a bleeding ulcer in the cardia (Figure 1b, Video 1) which was successfully treated with epinephrine (1:10,000) injections. Biopsies demonstrated nodular amyloid deposition (Figures 2) which was Congo red positive. The patient had no further hematemesis and was discharged home 4 days later. Ten months after autologous-SCT, EGD revealed a normal stomach (Figure 3, Video 2) with no histologic evidence of amyloid
We report a case of 59-year-old Turkish man with history of MVR and COPD whom was diagnosed with...
Hepatic involvement in AL amyloidosis may present as acute liver failure. Historically, liver transp...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
A 67-year-old woman with a incidental diagnosis of amyloidosis lambda subtype (AL-amyloid) presented...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
Patients with systemic amyloidosis often have symptoms related to impared gastrointestinal motility ...
Background: Hereditary transthyretin amyloid (ATTR) amyloidosis is a rare but fatal autosomal domina...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
A 45-year-old woman was diagnosed with myelodysplastic syndrome (MDS) with trisomy 8 and Behçet-like...
The gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but significant h...
SummaryThe gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but signif...
AL amyloidosis is an infiltrative disorder characterized by the extracellular deposition of insolubl...
Abstract Introduction Amyloidosis most often manifests as a systemic involvement of multiple tissues...
The gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but significant h...
We report a case of 59-year-old Turkish man with history of MVR and COPD whom was diagnosed with...
Hepatic involvement in AL amyloidosis may present as acute liver failure. Historically, liver transp...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...
Amyloidosis is a common complication of patients with monoclonal gammopathy of undetermined signific...
A 67-year-old woman with a incidental diagnosis of amyloidosis lambda subtype (AL-amyloid) presented...
Abstract Background Amyloidosis is characterized by extracellular tissue deposition of fibrils, comp...
Patients with systemic amyloidosis often have symptoms related to impared gastrointestinal motility ...
Background: Hereditary transthyretin amyloid (ATTR) amyloidosis is a rare but fatal autosomal domina...
We report this case of a 42-year-old woman who presented with a debilitating illness manifested by i...
A 45-year-old woman was diagnosed with myelodysplastic syndrome (MDS) with trisomy 8 and Behçet-like...
The gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but significant h...
SummaryThe gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but signif...
AL amyloidosis is an infiltrative disorder characterized by the extracellular deposition of insolubl...
Abstract Introduction Amyloidosis most often manifests as a systemic involvement of multiple tissues...
The gastrointestinal tract is frequently in involved light-chain (AL) amyloidosis, but significant h...
We report a case of 59-year-old Turkish man with history of MVR and COPD whom was diagnosed with...
Hepatic involvement in AL amyloidosis may present as acute liver failure. Historically, liver transp...
Systemic amyloidosis is a group of complex disorders characterized by the extracellular deposition o...