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十二指肠腺瘤中的胃十二指肠化生

Gastric duodenal metaplasia in duodenal adenomas.

作者信息

Rubio C A

机构信息

Gastrointestinal and Liver Pathology Research Laboratory, Department of Pathology Karolinska Institute and University Hospital, Stockholm, Sweden.

出版信息

J Clin Pathol. 2007 Jun;60(6):661-3. doi: 10.1136/jcp.2006.039388. Epub 2006 Jul 12.


DOI:10.1136/jcp.2006.039388
PMID:16837629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1955048/
Abstract

BACKGROUND: In cases of known aetiology, gastric duodenal metaplasia (GMD) is a reversible lesion. In cases of unknown aetiology, the fate of GMD remains elusive. GMD was recently found in a duodenal adenoma. AIM: To audit the frequency of GMD occurring in a cohort of duodenal adenomas. METHODS: Filed H&E-stained sections from 306 consecutive duodenal adenomas were investigated for the presence of GMD. RESULTS: 68% of the adenomas (n = 208) were from patients with familial adenomatous polyposis (FAP), and the remaining 32% (n = 98) were sporadic. GMD was found in 31.7% (66/208) of the duodenal FAP adenomas and in 59.2% (58/98) of the duodenal sporadic adenomas (p<0.05). The causes for this difference are elusive. CONCLUSIONS: As for other metaplasias of the gastrointestinal tract (intestinal metaplasia of the oesophagus and of the stomach, and metaplastic-hyperplastic polyposis of the colon, known to antedate neoplastic transformation), a subset of GMDs of unknown cause might be present in the duodenal mucosa before adenomatous changes ensue. That subset of GMD might have neoplastic proclivity similar to the metaplastic epithelium in other organs of the gastrointestinal tract. The known carcinogenic effect of high concentrations of bile acids and pancreatic juices bathing the duodenal mucosa carrying an irreversible subset of GDM might set aflame the adenomatous neoplastic transformation in these patients.

摘要

背景:在已知病因的情况下,胃十二指肠化生(GMD)是一种可逆性病变。在病因不明的情况下,GMD的转归仍不明确。最近在一例十二指肠腺瘤中发现了GMD。 目的:审查一组十二指肠腺瘤中GMD的发生频率。 方法:对306例连续的十二指肠腺瘤存档的苏木精-伊红(H&E)染色切片进行GMD检查。 结果:68%(n = 208)的腺瘤来自家族性腺瘤性息肉病(FAP)患者,其余32%(n = 98)为散发性。在31.7%(66/208)的十二指肠FAP腺瘤和59.2%(58/98)的十二指肠散发性腺瘤中发现了GMD(p<0.05)。这种差异的原因尚不清楚。 结论:至于胃肠道的其他化生(食管和胃的肠化生以及结肠的化生-增生性息肉病,已知先于肿瘤转化),在腺瘤性改变出现之前,十二指肠黏膜中可能存在一部分病因不明的GMD。那部分GMD可能具有与胃肠道其他器官的化生上皮相似的肿瘤倾向。高浓度胆汁酸和胰液对携带不可逆性GDM的十二指肠黏膜的已知致癌作用可能引发这些患者的腺瘤性肿瘤转化。

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