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Systemic Amyloidosis Manifested by Gastric Outlet Obstruction

机译:胃出口梗阻表现为系统性淀粉样变性

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摘要

Amyloidosis is characterized by extracellular deposition of insoluble protein fibrils that stain with Congo red application and appear apple green under polarized light. The presenting symptoms result from the involvement of many affected, nonspecific and generalized organ systems. Our patient was an 80-year-old woman with no medical history. She presented with a 2-week history of nausea and vomiting. An esophagogastroduodenoscopy showed erythematous and edematous mucosa on the antrum with pyloric stenosis. Histopathologic examination of the biopsy specimen showed the deposition of amorphous, homogeneous, and acidophilic material in the gastric mucosa. Amyloidal protein was proven by positive Congo red stain. A serum and urine immunfixation electrophoresis showed lambda light chain band. She developed symptoms of repeated greenish color vomiting. A follow-up esophagogastroduodenoscopy showed progressed antral obstruction. However, she refused further evaluation and treatment and was managed conservatively. She later died of disease progression after 34 hospital days.
机译:淀粉样变性病的特征是不溶性蛋白原纤维的细胞外沉积,该蛋白原纤维被刚果红染色并在偏振光下呈苹果绿。出现的症状是由于许多受影响的,非特异性的和广义的器官系统的参与所致。我们的患者是一名80岁的女性,没有病史。她有2周的恶心和呕吐史。食管胃十二指肠镜检查可见胃壁有红斑和水肿粘膜,并伴有幽门狭窄。活检标本的组织病理学检查显示无定形,均质和嗜酸性物质在胃粘膜中沉积。阳性刚果红染色证实了淀粉样蛋白。血清和尿液免疫固定电泳显示出λ轻链带。她出现反复绿色呕吐的症状。后续的食管胃十二指肠镜检查显示进展性肛门梗阻。但是,她拒绝进一步评估和治疗,并进行了保守治疗。她后来在医院住院34天后死于疾病进展。

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