Endoscopy 2015; 47(05): 437-443
DOI: 10.1055/s-0034-1391226
Original article
© Georg Thieme Verlag KG Stuttgart · New York

Confocal laser endomicroscopy for the differential diagnosis of ulcerative colitis and Crohn’s disease: a pilot study

Gian Eugenio Tontini
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
2   Gastroenterology and Digestive Endoscopy Unit, IRCCS Policlinico San Donato, San Donato Milanese, Italy
,
Jonas Mudter
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Michael Vieth
3   Institute of Pathology, Klinikum Bayreuth, Bayreuth, Germany
,
Raja Atreya
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Claudia Günther
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Yurdagül Zopf
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Dane Wildner
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Ralf Kiesslich
4   St. Marienkrankenhaus Katharina-Kasper, Frankfurt am Main, Germany
,
Maurizio Vecchi
2   Gastroenterology and Digestive Endoscopy Unit, IRCCS Policlinico San Donato, San Donato Milanese, Italy
5   Department of Biomedical Sciences for the Health, University of Milan, Milan, Italy
,
Markus F. Neurath
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
,
Helmut Neumann
1   Department of Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
› Author Affiliations
Further Information

Publication History

submitted 08 October 2013

accepted after revision 27 October 2014

Publication Date:
18 December 2014 (online)

Background and study aim: The differential diagnosis of ulcerative colitis from Crohn’s disease is of pivotal importance for the management of inflammatory bowel diseases, as both entities involve specific therapeutic management strategies. Confocal laser endomicroscopy (CLE) allows on-demand, in vivo characterization of architectural and cellular details during endoscopy. The aim of this study was to assess the efficacy of CLE to differentiate between ulcerative colitis and Crohn’s disease.

Patients and methods: This was a prospective study involving consecutive patients with a well-established diagnosis of ulcerative colitis or Crohn’s disease who underwent colonoscopy with fluorescein-aided confocal imaging.

Results: Overall, 79 patients were included (40 Crohn’s disease, 39 ulcerative colitis). CLE findings in patients with Crohn’s disease, showed significantly more discontinuous inflammation (87.5 % vs. 5.1 %), focal cryptitis (75.0 % vs. 12.8 %), and discontinuous crypt architectural abnormality (87.5 % vs. 10.3 %) than in ulcerative colitis (P < 0.0001). Conversely, ulcerative colitis was associated with severe, widespread crypt distortion (87.2 % vs. 17.5 % in Crohn’s disease), decreased crypt density (79.5 % vs. 22.5 %), and frankly irregular surface (89.7 % vs. 17.5 %; P < 0.0001 for all comparisons). Statistically significant differences were not seen for heavy, diffuse lamina propria cell increase or mucin preservation. No granulomas were visible. Based on these findings, a CLE scoring system was developed that revealed excellent accuracy (93.7 %) when compared with the historical clinical diagnosis and the histopathological gold standard.

Conclusions: CLE could visualize several disease-specific microscopic features, which are conventionally used in standard histopathology to differentiate between ulcerative colitis and Crohn’s disease. However, because of the limited penetration depth of CLE, submucosal details or granulomas were not visible. The new scoring system may allow in vivo diagnosis of ulcerative colitis or Crohn’s disease.

Trial registered at ClinicalTrials.gov: NCT 02238665

 
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