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   <subfield code="a">10.1007/s00535-011-0418-6</subfield>
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   <subfield code="a">Mucin phenotype and narrow-band imaging with magnifying endoscopy for differentiated-type mucosal gastric cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Masaaki Kobayashi, Manabu Takeuchi, Yoichi Ajioka, Satoru Hashimoto, Akito Sato, Rintaro Narisawa, Yutaka Aoyagi]</subfield>
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   <subfield code="a">Background: Several studies have described the surface glandular structure in differentiated early gastric cancer observed by narrow-band imaging with magnifying endoscopy (NBI-ME) in two main patterns, i.e., a papillary or granular structure in an intralobular loop pattern (ILL) and a pit structure in a fine network pattern (FNP). However, it is uncertain why the NBI-ME findings of differentiated-type carcinomas are divided into two main patterns. We investigated the significance of the mucin phenotype in the morphogenetic difference between ILL and FNP. Methods: We evaluated 120 intramucosal, well- or predominantly well-differentiated tubular adenocarcinomas. In each lesion, one area that showed the predominant pattern of microsurface structures and microvessels was selected and marked by electrocoagulation for a strict comparative study by NBI-ME and pathological investigation. NBI-ME findings were classified into three patterns: ILL, FNP, and intermediate. Mucin phenotypes were judged as gastric, intestinal, or gastrointestinal type by immunohistochemistry. Results: The mucin phenotype was gastric or gastrointestinal type in 24 (92.3%) of 26 ILL lesions. Intestinal phenotype was observed in 22 (84.6%) of 26 FNP lesions. The gastrointestinal phenotype was observed in 50 (73.5%) of 68 intermediate pattern lesions. The mucin phenotype and NBI-ME results were significantly correlated (P&lt;0.001). Conclusions: The mucin phenotype of differentiated early gastric cancer might be involved in morphogenetic differences between the papillary and pit structures visualized by NBI-ME.</subfield>
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   <subfield code="a">Springer, 2011</subfield>
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   <subfield code="a">Gastric phenotype</subfield>
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   <subfield code="a">Intestinal phenotype</subfield>
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   <subfield code="a">Intralobular loop pattern</subfield>
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   <subfield code="a">Kobayashi</subfield>
   <subfield code="D">Masaaki</subfield>
   <subfield code="u">Department of Endoscopy, Niigata University Medical and Dental Hospital, 1-757 Asahimachi-dori, Chuo-ku, 951-8510, Niigata, Japan</subfield>
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   <subfield code="a">Takeuchi</subfield>
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   <subfield code="u">Division of Gastroenterology and Hepatology, Niigata University Medical and Dental Hospital, Niigata, Japan</subfield>
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   <subfield code="a">Ajioka</subfield>
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   <subfield code="u">Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan</subfield>
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   <subfield code="a">Hashimoto</subfield>
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   <subfield code="u">Division of Gastroenterology and Hepatology, Niigata University Medical and Dental Hospital, Niigata, Japan</subfield>
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   <subfield code="a">Sato</subfield>
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   <subfield code="u">Division of Gastroenterology and Hepatology, Niigata University Medical and Dental Hospital, Niigata, Japan</subfield>
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   <subfield code="a">Narisawa</subfield>
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   <subfield code="u">Department of Endoscopy, Niigata University Medical and Dental Hospital, 1-757 Asahimachi-dori, Chuo-ku, 951-8510, Niigata, Japan</subfield>
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   <subfield code="u">Division of Gastroenterology and Hepatology, Niigata University Medical and Dental Hospital, Niigata, Japan</subfield>
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   <subfield code="t">Journal of Gastroenterology</subfield>
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   <subfield code="g">46/9(2011-09-01), 1064-1070</subfield>
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