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Adenocarcinoma with a Gastric Mucin Phenotype Arising from a Fundic Gland Polyp in a Patient with Familial Adenomatous Polyposis, Report of a Case Manabu Takeuchi 1 , Takashi Kato 2 , Masafumi Takatsuna 1 , Tomohiro Doi 1 , Hiroki Natsui 1 , Ryo Jinbo 1 , Itsuo Nagayama 1 , Keisuke Morita 1 , Yuji Kobayashi 1 , Seiichi Yoshikawa 1 , Hiroyuki Usuda 3 , 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 3Department of Pathology, Nagaoka Red Cross Hospital, Nagaoka, Japan Keyword: FAP , FGP , 胃型腫瘍 , 胃底腺粘膜型腺癌 , NBI pp.1585-1592
Published Date 2022/11/25
DOI https://doi.org/10.11477/mf.1403203053
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 A female in her 20s with familial adenomatous polyposis after total colectomy underwent endoscopy as part of her annual cancer surveillance. An endoscopic examination revealed a 7mm elevated lesion that was slightly reddish compared to the nearby fundic gland polyps. The biopsy specimens of the lesion revealed well- differentiated adenocarcinoma, therefore ESD(endoscopic submucosal dissection)was recommended. Magnifying narrow band imaging revealed an irregular microsurface pattern in areas with regular round pits, indicating a fundic gland polyp, and endocytoscopy revealed irregular glands with slight nuclear swelling, so we performed ESD on this lesion. This tumor was diagnosed histopathologically as adenocarcinoma(tub1, low), Type 0-I, pT1a(M), Ly0, V0, pHM0, pVM0, particularly gastric adenocarcinoma of fundic gland mucosa type based foveolar epithelial atypia and fundic gland dysplasia examined by immunohistochemical staining. It was a rare case in which a variant in not only dysplasia of the foveolar epithelium but also dysplasia of the fundic gland was recognized.


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

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