Microscopic colitis: Etiopathology, diagnosis, and rational management

  1. Ole Haagen Nielsen  Is a corresponding author
  2. Fernando Fernandez-Banares
  3. Toshiro Sato
  4. Darrell S Pardi
  1. Department of Gastroenterology, Herlev Hospital, University of Copenhagen, Denmark
  2. Department of Gastroenterology, Hospital Universitari Mutua Terrassa, Spain
  3. Centro de Investigación Biomédica en Red de enfermedades hepáticas y digestivas, Spain
  4. Department of Gastroenterology, Keio University School of Medicine, Japan
  5. Division of Gastroenterology and Hepatology, Mayo Clinic, United States
4 figures and 1 table

Figures

Geographic distribution of microscopic colitis in different parts of the world.

Most recent incidence rates (× 105 inhabitants per year) of both collagenous colitis (CC) and lymphocytic colitis (LC) from Europe and North America where population-based studies have been …

Main factors involved in the pathophysiology of microscopic colitis.
Histological findings of microscopic colitis.

(A) Typical colonic biopsy from a patient with collagenous colitis with a subepithelial collagenous band of more than 10 μM. The surface epithelium is flattened, and mucin depleted, and a mixed …

Proposed treatment algorithm for the clinical management of symptomatic microscopic colitis.

Immune checkpoint inhibitors (ICIs). *Loperamide or bismuth subsalicylate in mild cases, cholestyramine mainly if there is associated bile acid malabsorption. **Use the lowest effective dose as …

Tables

Table 1
Key histological findings in microscopic colitis: differences between collagenous and lymphocytic colitis.
ParameterCollagenous colitisLymphocytic colitis
Intraepithelial lymphocytesNormal or increased number>20 per 100 epithelial cells
Surface epitheliumMarked change (flattening, detachment)Slight change (vacuolization, flattening, mucin depletion)
Subepithelial collagenous bandThickening (≥10 μm)Normal or slightly increased (<10 μm)
Inflammatory infiltrate in the lamina propriaIncreased infiltrate (lymphocytes and plasma cells) with homogenous distribution throughout the colon
Crypt architectureLittle or no distortion
Inflammatory bowel disease-type focal changesOccasional cryptitis and Paneth cell metaplasia

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