Endoscopy 2011; 43(12): 1100-1104
DOI: 10.1055/s-0031-1291423
Case report/series
© Georg Thieme Verlag KG Stuttgart · New York

Usefulness of colonoscopic examination with indigo carmine in diagnosing microscopic colitis

G. Suzuki
1   Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
,
M. R. Mellander
1   Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
,
A. Suzuki
1   Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
,
C. A. Rubio
2   Department of Pathology, Karolinska University Hospital, Stockholm, Sweden
,
R. Lambert
3   Screening Group, Early Detection and Prevention, IARC, Lyon, France
,
J. Björk
1   Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
,
P. T. Schmidt
1   Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden
› Author Affiliations
Further Information

Publication History

submitted: 17 February 2011

accepted after revision: 11 July 2011

Publication Date:
04 November 2011 (online)

Microscopic colitis, comprising collagenous colitis and lymphocytic colitis, is epitomized by chronic watery diarrhea, endoscopically normal colonic mucosa, and characteristic histopathological features. Reports on chromoendoscopic findings in microscopic colitis are scarce and in this paper we describe such findings. We have examined 13 patients with microscopic colitis by means of chromoendoscopy with indigo carmine 0.2 % – 0.5 %. In all 13 cases continuous mucosal changes were seen, with disappearance of innominate grooves or with irregularity of grooves. The segmental distribution of abnormal chromoendoscopic findings corresponded almost completely with the microscopic features. A diffuse mosaic pattern was found in five of 10 cases of collagenous colitis and in all three cases of lymphocytic colitis. Uneven surface was seen in four cases of collagenous colitis, one of collagenous colitis in remission, and one of lymphocytic colitis, and a nodular surface was recorded in five cases of collagenous colitis but in none of the lymphocytic colitis cases. If these findings can be reproduced in larger series of microscopic colitis cases, the need for biopsies as a diagnostic tool might be restricted to patients where chromoendoscopy shows clear mucosal changes, thereby saving costs and limiting possible complications associated with multiple biopsies.

 
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