Intestinal-type gastric dysplasia in Helicobacter pylori-naive patients

被引:10
|
作者
Shibagaki, Kotaro [1 ]
Itawaki, Ayako [2 ]
Miyaoka, Yoichi [3 ]
Kishimoto, Kenichi [2 ]
Takahashi, Yusuke [2 ]
Kotani, Satoshi [2 ]
Mishiro, Tsuyoshi [2 ]
Oshima, Naoki [2 ]
Kawashima, Kousaku [2 ]
Ishimura, Norihisa [2 ]
Onuma, Hideyuki [4 ]
Nagasaki, Makoto [5 ]
Nagase, Mamiko [6 ]
Araki, Asuka [6 ]
Kadota, Kyuichi [6 ]
Kushima, Ryoji [7 ]
Ishihara, Shunji [2 ]
机构
[1] Shimane Univ Hosp, Dept Endoscopy, 89-1 Enya, Izumo, Shimane 6938501, Japan
[2] Shimane Univ, Fac Med, Dept Gastroenterol, Izumo, Shimane, Japan
[3] Shimane Prefectural Cent Hosp, Dept Gastroenterol, Izumo, Shimane, Japan
[4] Shimane Prefectural Cent Hosp, Dept Pathol, Izumo, Shimane, Japan
[5] Natl Hosp Org Hamada Med Ctr, Dept Pathol, Hamada, Japan
[6] Shimane Univ, Fac Med, Dept Pathol, Izumo, Shimane, Japan
[7] Shiga Univ Med Sci, Dept Pathol, Otsu, Shiga, Japan
关键词
Gastric cancer; Gastric dysplasia; Intestinal phenotype; Helicobacter pylori; p53; P53 PROTEIN EXPRESSION; FUNDIC GLAND TYPE; MAGNIFICATION ENDOSCOPY; CANCER; ADENOCARCINOMA; METAPLASIA; STOMACH; RISK; PHENOTYPE; INFECTION;
D O I
10.1007/s00428-021-03237-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastric dysplasia and gastric cancer in Helicobacter pylori (Hp)-naive patients usually exhibit a gastric phenotype, reflecting gastric mucosa without intestinal metaplasia (IM). We showed that intestinal-type gastric dysplasia (IGD) rarely occurs in the Hp-naive stomach. In the last 10 years, we treated 1760 gastric dysplasia and gastric cancer patients, with 3.6% (63/1760) being Hp-naive. Among these, ten were diagnosed with 14 IGDs and enrolled in this retrospective analysis. All lesions were observed by white-light endoscopy (WLE) and narrow-band imaging with magnification endoscopy (NBIME). We analyzed their endoscopic and microscopic features and patient demographics. Five men and five women aged 64 +/- 21 years were included. WLE showed the depressed lesions mimicking a benign raised erosion in the prepyloric compartment. Multiple growths were confirmed in 30% (3/10) of patients. NBIME showed a near-regular microstructure and capillaries in 50% (7/14) of lesions with a gastritis-like appearance. Histologically, background mucosa was non-atrophic pyloric gland tissue, but 40.0% of samples (4/10) contained sporadic IM. Most of the lesions (8/14) were low-grade dysplasia, and others had a high-grade component, with one progressing to intramucosal carcinoma. The neoplastic surface was widely covered with foveolar epithelium in 57.1% (8/14). Immunohistochemically, neoplastic cells expressed CDX2 in all patients (14/14), MUC2 and CD10 in 92.9% (13/14), MUC5AC in 14% (2/14), and no expression of MUC6, showing an intestinal phenotype. Ki-67 was overexpressed with a mean labeling index of 58.3 +/- 38.5%, and p-53 was overexpressed in 92.9% (13/14), regardless of the dysplastic grade. The IGD rarely occurs in Hp-naive patients with distinctive clinicopathologic characteristics.
引用
收藏
页码:783 / 792
页数:10
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