Kokkola A, Haapiainen R, Laxén F, Puolakkainen P, Kivilaakso E, Virtamo J, Sipponen P
Second Department of Surgery, Helsinki University Central Hospital, Finland.
J Clin Pathol. 1996 Dec;49(12):979-84. doi: 10.1136/jcp.49.12.979.
To assess the risk of gastric carcinoma in patients with histologically verified dysplasia and atrophic gastritis of the stomach.
One hundred and one patients with mild (n = 84), moderate (n = 14), or severe (n = 3) dysplasia among 359 elderly men who smoked underwent gastroscopy because of low serum pepsinogen. Patients with dysplasia were prospectively followed up for an average of four years with repeated gastroscopies and multiple biopsies.
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 spontaneously. 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 five cases, moderate or severe dysplasia recurred. Two of the three severe dysplasias progressed to carcinoma.
In atrophic gastritis progression of mild and moderate dysplastic lesions seems to be a slow process and is rare in mild dysplasia. However, severe dysplasia is 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 not progress. Severe dysplasia requires immediate surgical intervention.
评估经组织学证实患有胃发育异常和萎缩性胃炎患者的胃癌风险。
359名吸烟老年男性因血清胃蛋白酶原水平低接受胃镜检查,其中101例患有轻度(n = 84)、中度(n = 14)或重度(n = 3)发育异常。对发育异常患者进行前瞻性随访,平均随访四年,期间多次进行胃镜检查和多处活检。
84例轻度发育异常患者中有4例(4.8%)在随访期间进展为中度发育异常。大多数轻度发育异常病例自发缓解,无需手术干预。14例中度发育异常患者中有3例(21%)进展为重度发育异常,但随访期间未观察到癌变。5例中度发育异常病变通过手术或内镜切除。在这5例中的2例,中度或重度发育异常复发。3例重度发育异常中有2例进展为癌。
在萎缩性胃炎中,轻度和中度发育异常病变的进展似乎是一个缓慢的过程,轻度发育异常中很少见。然而,重度发育异常高度预示随后会发生癌症。建议轻度发育异常患者随访间隔为五年,中度发育异常患者为两年。中度发育异常需进行局部切除,但不能保证病变不会进展。重度发育异常需要立即进行手术干预。