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Adenocarcinoma of Gastric Fundic Mucosa Type with WOS Arising on a Background of Complete Intestinal Metaplasia, Report of a Case Manabu Takeuchi 1 , Yuji Kobayashi 1 , Masafumi Takatsuna 1 , Takashi Kato 2 , Yoichi Ajioka 2 1Department of Gastroenterology, Nagaoka Red Cross Hospital, Nagaoka, Japan 2Division of Molecular and Diagnostic Pathology, Niigata University, Graduate school of Medical and Dental Sciences, Niigata, Japan Keyword: 胃底腺粘膜型腺癌 , 腸上皮化生 , WOS , WGA , NBI pp.1707-1716
Published Date 2024/11/25
DOI https://doi.org/10.11477/mf.1403203782
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 A male patient aged 70 years presented with an erythematous, rising, steeply elevated lesion of 12mm in size on the anterior wall of the gastric lower body. Narrow-band imaging(NBI)at magnification detected small and irregularly sized granular and papillary structures with white opaque substance(WOS). The background mucosa was villous with scattered white globe changes similar to white globe appearance(WGA). Histopathological examination revealed mucin 2(MUC2)and CD10-positive complete intestinal metaplasia in the background mucosa, MUC5AC-positive foveolar epithelium-like atypical ducts in the superficial layer of the tumor, and irregularly branching and dilated pepsinogen I- and MUC6-positive atypical ducts in the subepithelium, resulting in the diagnosis of adenocarcinoma of gastric fundic mucosa type. Both WOS and WGA-like areas were adipophilin-positive fatty plaques located in the epithelium in WOS and the subepithelial stroma in WGA, confirming the vascular findings on NBI magnification. Most gastric fundic mucosal adenocarcinomas originate from the gastric fundic gland without atrophy. WOS, which is observed in gastric epithelial tumors, frequently presents as an intestinal mucin phenotype. However, this lesion demonstrates a complete intestinal metaplasia of the background mucosa and exhibits a gastric mucin phenotype, which is crucial.


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