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Multicenter Study
. 2004 Mar;53(3):381-6.
doi: 10.1136/gut.2003.027771.

Duodenal adenomatosis in familial adenomatous polyposis

S Bülow  1 , J Björk, I J Christensen, O Fausa, H Järvinen, F Moesgaard, H F A Vasen; DAF Study Group
Affiliations
Multicenter Study

Duodenal adenomatosis in familial adenomatous polyposis

S Bülow et al. Gut. 2004 Mar.

Abstract

Background: The prevalence of duodenal carcinoma is much higher in familial adenomatous polyposis (FAP) than in the background population, and duodenal adenomatosis is found in most polyposis patients.

Aims: To describe the long term natural history of duodenal adenomatosis in FAP and evaluate if cancer prophylactic surveillance of the duodenum is indicated.

Methods: A prospective five nation study was carried out in the Nordic countries and the Netherlands.

Patients: A total of 368 patients were examined by gastroduodenoscopy at two year intervals during the period 1990-2001.

Results: At the first endoscopy, 238 (65%) patients had duodenal adenomas at a median age of 38 years. Median follow up was 7.6 years. The cumulative incidence of adenomatosis at age 70 years was 90% (95% confidence interval (CI) 79-100%), and of Spigelman stage IV 52% (95% CI 28-76%). The probability of an advanced Spigelman score increased during the study period (p<0.0001) due to an increasing number and size of adenomas. Two patients had asymptomatic duodenal carcinoma at their first endoscopy while four developed carcinoma during the study at a median age of 52 years (range 26-58). The cumulative incidence rate of cancer was 4.5% at age 57 years (95% CI 0.1-8.9%) and the risk was higher in patients with Spigelman stage IV at their first endoscopy than in those with stages 0-III (p<0.01).

Conclusions: The natural course of duodenal adenomatosis has now been described in detail. The high incidence and increasing severity of duodenal adenomatosis with age justifies prophylactic examination, and a programme is presented for upper gastrointestinal endoscopic surveillance.

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Figures

Figure 1
Figure 1
Spigelman classification in classifiable patients in relation to time after entry into the study.
Figure 2
Figure 2
Cumulative incidence of adenomatosis development.
Figure 3
Figure 3
Cumulative incidence of Spigelman stage IV.
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