Long-term follow-up in atrophic body gastritis patients:: atrophy and intestinal metaplasia are persistent lesions irrespective of Helicobacter pylori infection

被引:95
作者
Lahner, E
Bordi, C
Cattaruzza, MS
Iannoni, C
Milione, M
Delle Fave, G
Annibale, B
机构
[1] Univ Roma La Sapienza, Sch Med 2, Digest & Liver Dis Unit, Rome, Italy
[2] Univ Parma, Pathol Unit, I-43100 Parma, Italy
[3] Univ Roma La Sapienza, Clin Epidemiol Unit, Rome, Italy
[4] Univ Roma La Sapienza, Dept Clin Sci, Pathol Unit, Rome, Italy
关键词
D O I
10.1111/j.1365-2036.2005.02582.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Long-term outcome of atrophic body gastritis has not yet been defined. Aims: To investigate at long-term follow-up the behaviour of atrophy and intestinal metaplasia and the occurrence of neoplastic lesions in atrophic body gastritis patients. Methods: Overall 106 atrophic body gastritis patients with >= 4-year follow-up were studied; 38 were Helicobacter pylori-positive at histology + serology and cured of infection (group A), 36 were positive at serology and not treated (group B) and 32 were H. pylori-negative (group C). Patients underwent gastroscopy with antral (n = 3) and body (n = 3) biopsies for histology according to the Sydney System. Results: At 6.7-year follow-up body atrophy and intestinal metaplasia remained unchanged in all 106 patients irrespective of H. pylori status. Antral atrophy was significantly increased at follow-up only in group C, whereas antral intestinal metaplasia was unchanged in all three groups. During follow-up eight (8%) patients developed neoplastic lesions (one adenocarcinoma, one adenoma with low-grade dysplasia and six low-grade dysplasia without endoscopic lesions). Antral atrophic gastritis was present at baseline in all but one (88%) of the eight patients with neoplastic lesions, but only in 15 (15%) of the 98 patients without (P < 0.0001, RR = 26.7). Conclusions: Atrophy and intestinal metaplasia persist at 6.7-year follow-up and atrophic body gastritis patients with panatrophic gastritis are at increased risk of developing neoplastic lesions.
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页码:471 / 481
页数:11
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