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DOI 10.1111/j.1365-2036.2005.02401.x

Медицинская библиотека · Alimentary pharmacology & therapeutics · 2005

High-grade dysplasia in Barrett's oesophagus: natural history and review of clinical practice.

Thomas T, Richards C J, de Caestecker J S, Robinson R J

СтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Management of high-grade dysplasia in Barrett's oesophagus is controversial: surgery carries an appreciable morbidity/mortality, high-grade dysplasia may not progress to cancer and endoscopic ablation is an emerging option.

AIM: To review Barrett's oesophagus-related high-grade dysplasia management and outcome over a 10-year period.

METHODS

This was a retrospective case note review of 36 patients identified from a pathology database.

RESULTS

There were 31 men of mean age 67 years. Endoscopic surveillance identified nine. Median follow-up was 21 months. Seven patients had no further intervention because of age/comorbidity. The other 29 had repeat endoscopic biopsies, nine showing cancer (six oesophagectomized). Of the 20 remaining patients with persisting high-grade dysplasia, eight had surgery (histology showed cancer in six), seven continued endoscopic surveillance (high-grade dysplasia regressed in four) and five had 'curative' argon ablation. An intensive biopsy protocol was not followed in 55% of endoscopies. Prevalent cancers occurred in 44% with an annual incidence of 5% over 5 years. All cause mortality was 39% (14 of 36, eight of 14 from cancer).

CONCLUSIONS

Management of high-grade dysplasia was not uniform. Unsuspected cancer was common in high-grade dysplasia patients undergoing surgery but 13% regressed under surveillance. High-grade dysplasia patients have a high mortality but 43% did not die from cancer.

Для цитирования: Thomas T, Richards C J, de Caestecker J S, Robinson R J. High-grade dysplasia in Barrett's oesophagus: natural history and review of clinical practice.. Alimentary pharmacology & therapeutics. 2005. DOI: 10.1111/j.1365-2036.2005.02401.x.

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