A. Kokkola et al., RISK OF GASTRIC-CARCINOMA IN PATIENTS WITH MUCOSAL DYSPLASIA ASSOCIATED WITH ATROPHIC GASTRITIS - A FOLLOW-UP-STUDY, Journal of Clinical Pathology, 49(12), 1996, pp. 979-984
Aims-To assess the risk of gastric carcinoma in patients with histolog
ically verified dysplasia and atrophic gastritis of the stomach. Metho
ds-One hundred and one patients with mild (n = 84), moderate (n = 14),
or severe (n = 3) dysplasia among 359 elderly men who smoked underwen
t gastroscopy because of low serum pepsinogen. Patients with dysplasia
were prospectively followed up for an average of four years with repe
ated gastroscopies and multiple biopsies. Results-Four of the 84 (4.8%
) cases of mild dysplasia had progressed to moderate dysplasia during
the follow up. Most of the cases of mild dysplasia had resolved sponta
neously. No surgical intervention was required. Three of the 14 (21%)
cases of moderate dysplasia had progressed to severe dysplasia, but no
carcinomas were observed during follow up. Five moderately dysplastic
lesions were removed surgically or endoscopically. In two of these fi
ve cases, moderate or severe dysplasia recurred. Two of the three seve
re dysplasias progressed to carcinoma. Conclusions-In atrophic gastrit
is progression of mild and moderate dysplastic lesions seems to be a s
low process and is rare in mild dysplasia. However, severe dysplasia i
s highly predictive of subsequent cancer. It is suggested that a five
year follow up interval is sufficient in cases with mild dysplasia and
two years in those with moderate dysplasia. Local removal of moderate
dysplasia is indicated but does not guarantee that the lesion will no
t progress. Severe dysplasia requires immediate surgical intervention.