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Presentation, treatment and outcome in patients with ampullary tumours

✍ Scribed by V. Bettschart; M. Q. Rahman; F. J. F. Engelken; K. K. Madhavan; R. W. Parks; O. J. Garden


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
145 KB
Volume
91
Category
Article
ISSN
0007-1323

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✦ Synopsis


Abstract

Background

Ampullary tumours are relatively rare, and few large single-centre reports provide information on their treatment and outcome. The aim of this study was to analyse outcome and determine predictors of survival for patients with ampullary tumours treated in a specialist centre.

Methods

Over an 11-year period, 561 patients were treated for periampullary tumours, 88 of whom had a histologically proven ampullary neoplasm. Prospectively gathered data were analysed to assess predictors of survival.

Results

The overall resection rate was 92 per cent; there were no postoperative deaths. Median survival was 45Β·8 months for patients with resectable tumours and 8Β·0 months for those with irresectable disease (P < 0Β·001). On univariate analysis, age less than 70 years (P = 0Β·015) and a bilirubin level of 75 Β΅mol/l or less (P = 0Β·012) favoured long-term survival. Among 70 patients who underwent cancer resection, factors associated with significantly worse long-term survival on univariate analysis included poorly differentiated tumour (P < 0Β·001), positive nodes (P < 0Β·001), perineural invasion (P = 0Β·001) and invasion of the pancreas (P = 0Β·018). Multivariate analysis identified positive nodes and bilirubin concentration as independent predictors of survival.

Conclusion

An aggressive surgical approach to ampullary tumours is justified by the low proportion of benign lesions, the absence of postoperative mortality and improved long-term survival.


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