Japanese

Localized AL Amyloidosis of the Stomach with IIa-like Endoscopic Appearance, Report of a Case Naotoshi Sugimoto 1 , Hiroyuki Narahara 1 , Hiroyasu Iishi 1 , Hideharu Ogiyama 1 , Takuya Yamada 1 1Departments of Gastrointestinal Oncology, Osaka Medical Center for Cancer and Cardiovascular Diseases Keyword: 胃アミロイドーシス , AL型 , 内視鏡 pp.1321-1325
Published Date 2005/8/25
DOI https://doi.org/10.11477/mf.1403100156
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A 58-year-old woman was referred to our hospital because of an abnormality in the gastric corpus detected during mass screening. Radiological and endoscopic examinations of the gastrointestinal tract showed a localized elevated lesion covered with coarse mucosa on the lesser curvature in the corpus. Histological examination of the biopsy specimens revealed amyloid deposits of AL type in the mucosal layer. No other organs were affected by amyloidosis. Relying on these findings we diagnosed the disorder as AL amyloidosis localized to the stomach. There has been no obvious progression during the six years since the first medical examination.

Diseases, Osaka, Japan


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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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