Background and Study Aims: Recent data suggest that panchromoscopy using methylene blue can improve the detection
of intraepithelial neoplastic lesions in the context of surveillance colonoscopy for
patients with chronic ulcerative colitis. This method has also been shown to provide
a more accurate diagnosis of the extent of disease and inflammatory activity. Interval
cancers are known to occur in patients with chronic ulcerative colitis despite the
adoption of currently accepted surveillance biopsy protocols. We hypothesised that
targeted chromoscopy alone, with high-magnification imaging, may increase the total
number of intraepithelial neoplastic lesions detected, compared with conventional
colonoscopy and biopsy surveillance according to current protocols.
Patients and Methods: A total of 350 patients with long-standing ulcerative colitis (≥ 8 years) underwent
surveillance colonoscopy using high-magnification chromoscopic colonoscopy (HMCC).
Quadrantic biopsies at 10-cm intervals were taken on extubation in addition to targeted
biopsies of abnormal mucosal areas. Defined lesions were further evaluated using modified
Kudo crypt pattern analysis. These data were compared with data from 350 disease duration-
and disease extent-matched control patients who had undergone conventional colonoscopic
surveillance between January 2001 and April 2005.
Results: Significantly more intraepithelial neoplastic lesions were detected in the magnification
chromoscopy group compared with controls (69 vs. 24, P < 0.0001). Intraepithelial neoplasia was observed in 67 lesions, of which 53 (79
%) were detected using magnification chromoscopy alone. Chromoscopy increased the
number of flat lesions with intraepithelial neoplasia detected compared with controls
(P < 0.001). Twenty intraepithelial neoplastic lesions were detected from 12 850 non-targeted
biopsies in the HMCC group (0.16 %), while 49 intraepithelial neoplastic lesions were
detected from the 644 targeted biopsies in the HMCC group (8 %). From 12 482 non-targeted
biopsies taken in the control group patients, 18 (0.14 %) showed intraepithelial neoplasia.
The yield of intraepithelial neoplastic lesions from targeted biopsies in the control
group (i. e. without HMCC imaging), however, was only modestly improved at 1.6 % (6/369).
Using modified Kudo criteria, the sensitivity and specificity for differentiating
neoplastic from non-neoplastic lesions using HMCC were 93 % and 88 % respectively.
The total procedure time was significantly longer in the HMCC group compared with
controls (P < 0.02).
Conclusions: Magnification chromoscopy improves the detection of intraepithelial neoplasia in
the endoscopic screening of patients with chronic ulcerative colitis. Neoplastic and
non-neoplastic mucosal change can be predicted with a high overall accuracy using
magnification techniques. These adjunctive endoscopic techniques have important clinical
implications and may lead to changes in current practice guidelines.
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D. P. Hurlstone, M. D.
Gastroenterology and Liver Unit, The Royal Hallamshire Hospital ·
17 Alexandra Gardens · Lyndhurst Road · Nether Edge · Sheffield, S11 9DQ · United
Kingdom·
Fax: +44-114-2712692
Email: p.hurlstone@shef.ac.uk