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首页> 外文期刊>Journal of Medical Case Reports >Localized gastric amyloidosis differentiated histologically from scirrhous gastric cancer using endoscopic mucosal resection: a case report
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Localized gastric amyloidosis differentiated histologically from scirrhous gastric cancer using endoscopic mucosal resection: a case report

机译:内镜下黏膜切除术在局部胃淀粉样变性与硬化性胃癌的组织学区别

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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 deposits in the submucosal layer with no malignant findings. We resected a representative portion of the lesion by endoscopic mucosal resection using the strip biopsy method to obtain sufficient tissue specimens, and then conducted a detailed histological evaluation of the samples. The resected specimens revealed deposition of amyloidal materials in the gastric mucosa and submucosa without any malignant findings. Congo red staining results were positive for amyloidal protein and exhibited green birefringence under polarized light. Congo red staining with prior potassium permanganate incubation confirmed the light chain (AL) amyloid protein type. Based on these results, gastric malignancy, systemic amyloidosis and amyloid deposits induced by inflammatory disease were excluded and this lesion was consequently diagnosed as localized gastric amyloidosis. Our patient was an older woman and there were no findings relative to an increase in gastrointestinal symptoms or anemia, so no further treatment was performed. She continued to be in good condition without any finding of disease progression six years after verification of our diagnosis. Conclusions We report an unusual case of primary amyloidosis of the stomach resembling scirrhous gastric carcinoma. This case of localized gastric amyloidosis was differentiated from scirrhous gastric cancer after performing endoscopic mucosal resection without an invasive surgical resection, as endoscopic mucosal resection provided sufficient tissue specimens from the lesion to make an accurate histological evaluation.
机译:简介淀粉样变性最常表现为多种组织和器官的全身性受累,而局限于胃部的淀粉样沉积极为罕见。有时很难通过活检标本明确诊断出局限性胃淀粉样变性病,并且在某些情况下,只有在手术切除胃后才能最终确定淀粉样变性病的诊断。病例介绍一名76岁的日本上腹部不适的妇女接受了食管胃十二指肠镜检查。食管胃十二指肠镜检查显示胃壁增厚,提示为硬化性胃癌,从胃体的上部到下部弯曲较大。活检标本显示淀粉样蛋白沉积在粘膜下层,无恶性发现。我们使用带状活检方法通过内窥镜黏膜切除术切除了病变的代表性部分,以获得足够的组织样本,然后对样本进行了详细的组织学评估。切除的标本显示淀粉样物质沉积在胃粘膜和粘膜下层,无任何恶性发现。刚果红染色对淀粉样蛋白呈阳性,在偏振光下显示绿色双折射。刚果红染色与先前的高锰酸钾孵育确定了轻链(AL)淀粉样蛋白类型。基于这些结果,排除了由恶性疾病引起的胃恶性肿瘤,全身性淀粉样变性病和淀粉样蛋白沉积物,因此将该病变诊断为局部性胃淀粉样变性病。我们的患者是一名老年妇女,没有发现与胃肠道症状或贫血增加有关的发现,因此未进行进一步治疗。证实我们的诊断后六年,她仍然处于良好状态,没有发现任何疾病进展。结论我们报告了罕见的原发性胃淀粉样变性病,类似于肝硬化性胃癌。内镜黏膜切除术无创手术切除后,这种局限性胃淀粉样变性病例与硬化性胃癌有所区别,因为内镜黏膜切除术可从病变处提供足够的组织标本以进行准确的组织学评估。

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