Lymphocytic follicles and aggregates are a determinant of mucosal damage and duration of diarrhea

Arch Pathol Lab Med. 2013 Jan;137(1):83-9. doi: 10.5858/arpa.2011-0430-OA.

Abstract

Context: Nonspecific changes (nonspecific chronic inflammation) in patients with chronic diarrhea represent the commonest diagnosis in colorectal biopsy interpretation, but these changes are of little clinical significance.

Objective: To find, within this group, histologic and immunohistologic diagnostic criteria to predict the duration and resolution of diarrhea.

Design: Detailed clinical features and histologic findings were analyzed in a cohort of 47 patients with chronic diarrhea, with near-normal histology and no clear-cut known etiologic agent. Immunohistochemistry to mast cells (CD117) and Treg cells (FOXP3) was also assessed in 39 patients.

Results: Increased number of lymphoid follicles and aggregates, increased number of mast cells, and paucity of Treg were the statistically significant key findings (P = .003, P = .008, and P = .04, respectively). The duration of diarrhea was correlated with the number of large lymphoid follicles and aggregates (P = .001, r = .48), number of total lymphoid follicles and aggregates (P = .003, r = .43), density of lymphoid follicles and aggregates (P = .009, r = .38), and total lymphoid follicles and aggregates per biopsy (P = .004, r = .42) and the number of mast cells (P = .001, r = .52). The number of mast cells and Treg cells showed significant difference between resolved and unresolved cases (P = .001 and P = .01 respectively).

Conclusions: Lymphocytic follicles and aggregates colitis, previously regarded as of negligible diagnostic significance, allows the prediction of the behavior of chronic diarrhea in a subset of patients with nonspecific changes on colonic biopsy. The increased number of mast cells and paucity of Treg cells further helps to identify such unresolved cases.

MeSH terms

  • Adult
  • Aged
  • Biopsy
  • Case-Control Studies
  • Chronic Disease
  • Cohort Studies
  • Diarrhea / immunology
  • Diarrhea / metabolism
  • Diarrhea / pathology*
  • Female
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Immunity, Mucosal
  • Immunohistochemistry
  • Inflammation / metabolism
  • Inflammation / pathology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology*
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / metabolism
  • Lymphoid Tissue / pathology*
  • Male
  • Middle Aged
  • Proto-Oncogene Proteins c-kit / metabolism
  • Time Factors
  • Young Adult

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Proto-Oncogene Proteins c-kit