Department of Endoscopy, Niigata University Medical and Dental Hospital, 1-757 Asahimachi-dori, Chuo-ku, Niigata 951-8510, Japan.
J Gastroenterol. 2011 Sep;46(9):1064-70. doi: 10.1007/s00535-011-0418-6. Epub 2011 Jun 11.
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.
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.
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 < 0.001).
The mucin phenotype of differentiated early gastric cancer might be involved in morphogenetic differences between the papillary and pit structures visualized by NBI-ME.
几项研究描述了窄带成像放大内镜(NBI-ME)观察到的分化型早期胃癌的表面腺状结构,主要有两种模式,即小叶内环形模式(ILL)的乳头状或颗粒状结构和精细网络模式(FNP)的凹陷结构。然而,尚不清楚为什么 NBI-ME 对分化型癌的发现分为两种主要模式。我们研究了黏液表型在 ILL 和 FNP 形态差异中的意义。
我们评估了 120 例黏膜内、高分化或中分化管状腺癌。在每个病变中,选择一个主要显示微表面结构和微血管模式的区域,并用电凝标记,以便通过 NBI-ME 和病理研究进行严格的对比研究。NBI-ME 结果分为 ILL、FNP 和中间型三种类型。通过免疫组织化学判断黏液表型为胃型、肠型或胃肠型。
26 个 ILL 病变中有 24 个(92.3%)为胃型或胃肠型黏液表型。26 个 FNP 病变中有 22 个(84.6%)为肠型黏液表型。在 68 个中间型病变中有 50 个(73.5%)为胃肠型黏液表型。黏液表型和 NBI-ME 结果呈显著相关(P<0.001)。
分化型早期胃癌的黏液表型可能与 NBI-ME 观察到的乳头状和凹陷结构的形态发生差异有关。