Microscopic colitis: clinical findings, topography and persistence of histopathological subgroups

Aliment Pharmacol Ther 2011; 34: 1225–1234 Summary Background  Uncertainty remains on topography and persistence of histological subgroups of microscopic colitis (MC). Aim  To assess longitudinal clinical, endoscopic, histological, and therapeutic description of MC subgroups including patients with...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2011-11, Vol.34 (10), p.1225-1234
Hauptverfasser: Bjørnbak, C., Engel, P. J. H., Nielsen, P. L., Munck, L. K.
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container_issue 10
container_start_page 1225
container_title Alimentary pharmacology & therapeutics
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creator Bjørnbak, C.
Engel, P. J. H.
Nielsen, P. L.
Munck, L. K.
description Aliment Pharmacol Ther 2011; 34: 1225–1234 Summary Background  Uncertainty remains on topography and persistence of histological subgroups of microscopic colitis (MC). Aim  To assess longitudinal clinical, endoscopic, histological, and therapeutic description of MC subgroups including patients with incomplete findings of MC (MCi). Methods  Retrospective review of a consecutive cohort with MC and histological reassessment of MCi. Results  Clinical characteristics of 168 patients with lymphocytic colitis (LC), 270 with collagenous colitis (CC) and 101 with MCi were similar. At colonoscopy 95% (95% CI: 91–98%) of CC and 98% (93–100%) of LC cases had diagnostic histopathology of MC in both left and right colon. Eight and three patients had characteristics of MC only in the left and right colon, respectively. Histology findings resembling coexistence of the other MC subtype was present in 48% (40–55%) with CC and 24% (18–31%) with LC. A first diagnosis of MC was made in 49 (30%) of 164 patients only at repeat endoscopy. Another 34 of 115 (30%) with MC in the first endoscopy did not fulfil the MC criteria at repeat endoscopy. Only seven cases had a primary endoscopy without histopathological abnormalities. Fifteen percentage of MCi were reclassified as MC. Ileal inflammation was present in 33 of 81 patients. Budesonide was efficacious in all MC subgroups irrespective of bile acid malabsorption. Conclusions  Clinical characteristics of microscopic colitis subgroups are indistinguishable. Biopsies from the left colon suffice to exclude microscopic colitis, and the histological diagnosis of microscopic colitis is inconsistent over time. Ileal inflammation is common. The term microscopic colitis should perhaps be considered one clinical entity and include lymphocytic colitis, collagenous colitis, and incomplete findings of microscopic colitis.
doi_str_mv 10.1111/j.1365-2036.2011.04865.x
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J. H. ; Nielsen, P. L. ; Munck, L. K.</creator><creatorcontrib>Bjørnbak, C. ; Engel, P. J. H. ; Nielsen, P. L. ; Munck, L. K.</creatorcontrib><description>Aliment Pharmacol Ther 2011; 34: 1225–1234 Summary Background  Uncertainty remains on topography and persistence of histological subgroups of microscopic colitis (MC). Aim  To assess longitudinal clinical, endoscopic, histological, and therapeutic description of MC subgroups including patients with incomplete findings of MC (MCi). Methods  Retrospective review of a consecutive cohort with MC and histological reassessment of MCi. Results  Clinical characteristics of 168 patients with lymphocytic colitis (LC), 270 with collagenous colitis (CC) and 101 with MCi were similar. At colonoscopy 95% (95% CI: 91–98%) of CC and 98% (93–100%) of LC cases had diagnostic histopathology of MC in both left and right colon. Eight and three patients had characteristics of MC only in the left and right colon, respectively. Histology findings resembling coexistence of the other MC subtype was present in 48% (40–55%) with CC and 24% (18–31%) with LC. A first diagnosis of MC was made in 49 (30%) of 164 patients only at repeat endoscopy. Another 34 of 115 (30%) with MC in the first endoscopy did not fulfil the MC criteria at repeat endoscopy. Only seven cases had a primary endoscopy without histopathological abnormalities. Fifteen percentage of MCi were reclassified as MC. Ileal inflammation was present in 33 of 81 patients. Budesonide was efficacious in all MC subgroups irrespective of bile acid malabsorption. Conclusions  Clinical characteristics of microscopic colitis subgroups are indistinguishable. Biopsies from the left colon suffice to exclude microscopic colitis, and the histological diagnosis of microscopic colitis is inconsistent over time. Ileal inflammation is common. The term microscopic colitis should perhaps be considered one clinical entity and include lymphocytic colitis, collagenous colitis, and incomplete findings of microscopic colitis.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/j.1365-2036.2011.04865.x</identifier><identifier>PMID: 21967618</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Biological and medical sciences ; Biopsy ; Cohort Studies ; Colitis, Microscopic - diagnosis ; Colonoscopy - methods ; Diagnosis, Differential ; Diarrhea - pathology ; Digestive system ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Male ; Medical sciences ; Middle Aged ; Pharmacology. 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J. H.</creatorcontrib><creatorcontrib>Nielsen, P. L.</creatorcontrib><creatorcontrib>Munck, L. K.</creatorcontrib><title>Microscopic colitis: clinical findings, topography and persistence of histopathological subgroups</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Aliment Pharmacol Ther 2011; 34: 1225–1234 Summary Background  Uncertainty remains on topography and persistence of histological subgroups of microscopic colitis (MC). Aim  To assess longitudinal clinical, endoscopic, histological, and therapeutic description of MC subgroups including patients with incomplete findings of MC (MCi). Methods  Retrospective review of a consecutive cohort with MC and histological reassessment of MCi. Results  Clinical characteristics of 168 patients with lymphocytic colitis (LC), 270 with collagenous colitis (CC) and 101 with MCi were similar. At colonoscopy 95% (95% CI: 91–98%) of CC and 98% (93–100%) of LC cases had diagnostic histopathology of MC in both left and right colon. Eight and three patients had characteristics of MC only in the left and right colon, respectively. Histology findings resembling coexistence of the other MC subtype was present in 48% (40–55%) with CC and 24% (18–31%) with LC. A first diagnosis of MC was made in 49 (30%) of 164 patients only at repeat endoscopy. Another 34 of 115 (30%) with MC in the first endoscopy did not fulfil the MC criteria at repeat endoscopy. Only seven cases had a primary endoscopy without histopathological abnormalities. Fifteen percentage of MCi were reclassified as MC. Ileal inflammation was present in 33 of 81 patients. Budesonide was efficacious in all MC subgroups irrespective of bile acid malabsorption. Conclusions  Clinical characteristics of microscopic colitis subgroups are indistinguishable. Biopsies from the left colon suffice to exclude microscopic colitis, and the histological diagnosis of microscopic colitis is inconsistent over time. Ileal inflammation is common. The term microscopic colitis should perhaps be considered one clinical entity and include lymphocytic colitis, collagenous colitis, and incomplete findings of microscopic colitis.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Cohort Studies</subject><subject>Colitis, Microscopic - diagnosis</subject><subject>Colonoscopy - methods</subject><subject>Diagnosis, Differential</subject><subject>Diarrhea - pathology</subject><subject>Digestive system</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. 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H.</creatorcontrib><creatorcontrib>Nielsen, P. L.</creatorcontrib><creatorcontrib>Munck, L. K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bjørnbak, C.</au><au>Engel, P. J. H.</au><au>Nielsen, P. L.</au><au>Munck, L. K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microscopic colitis: clinical findings, topography and persistence of histopathological subgroups</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2011-11</date><risdate>2011</risdate><volume>34</volume><issue>10</issue><spage>1225</spage><epage>1234</epage><pages>1225-1234</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Aliment Pharmacol Ther 2011; 34: 1225–1234 Summary Background  Uncertainty remains on topography and persistence of histological subgroups of microscopic colitis (MC). Aim  To assess longitudinal clinical, endoscopic, histological, and therapeutic description of MC subgroups including patients with incomplete findings of MC (MCi). Methods  Retrospective review of a consecutive cohort with MC and histological reassessment of MCi. Results  Clinical characteristics of 168 patients with lymphocytic colitis (LC), 270 with collagenous colitis (CC) and 101 with MCi were similar. At colonoscopy 95% (95% CI: 91–98%) of CC and 98% (93–100%) of LC cases had diagnostic histopathology of MC in both left and right colon. Eight and three patients had characteristics of MC only in the left and right colon, respectively. Histology findings resembling coexistence of the other MC subtype was present in 48% (40–55%) with CC and 24% (18–31%) with LC. A first diagnosis of MC was made in 49 (30%) of 164 patients only at repeat endoscopy. Another 34 of 115 (30%) with MC in the first endoscopy did not fulfil the MC criteria at repeat endoscopy. Only seven cases had a primary endoscopy without histopathological abnormalities. Fifteen percentage of MCi were reclassified as MC. Ileal inflammation was present in 33 of 81 patients. Budesonide was efficacious in all MC subgroups irrespective of bile acid malabsorption. Conclusions  Clinical characteristics of microscopic colitis subgroups are indistinguishable. Biopsies from the left colon suffice to exclude microscopic colitis, and the histological diagnosis of microscopic colitis is inconsistent over time. Ileal inflammation is common. The term microscopic colitis should perhaps be considered one clinical entity and include lymphocytic colitis, collagenous colitis, and incomplete findings of microscopic colitis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21967618</pmid><doi>10.1111/j.1365-2036.2011.04865.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Biological and medical sciences
Biopsy
Cohort Studies
Colitis, Microscopic - diagnosis
Colonoscopy - methods
Diagnosis, Differential
Diarrhea - pathology
Digestive system
Female
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Retrospective Studies
title Microscopic colitis: clinical findings, topography and persistence of histopathological subgroups
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