Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8807435 | Human Pathology | 2018 | 28 Pages |
Abstract
Intestinal stricture, a major complication of Crohn's disease (CD), results from fibromuscular remodeling and expansion of the intestinal wall. The corresponding microanatomical alterations have not been fully described, hindering progress toward understanding their pathogenesis and devising appropriate treatments. We used tissue-specific staining and quantitative digital histomorphometry for this purpose. Serial histologic sections from 37 surgically resected ileal strictures and adjacent nonstrictured controls from patients with CD were evaluated after staining for smooth muscle actin, collagen (Sirius red), and collagen types I, III, and V. Overall mural thickening in strictures was increased 2.2â¯Â±â¯0.2-fold compared with nonstrictured regions of the same specimens. The muscular layer most altered was the muscularis mucosae (MM). Compared with the internal and external layers of the muscularis propria, (MP) which were expanded 1.9â¯Â±â¯0.2- and 1.3â¯Â±â¯0.1-fold, respectively, the MM was expanded 17.7â¯Â±â¯2.6-fold, reflecting the combined effects of architectural disarray, an 11.6â¯Â±â¯1.4-fold increase smooth muscle content, and elaboration of pericellular type V collagen. In contrast, the architecture of the MP was preserved and pericellular collagen was virtually absent; rather, fibrosis in this layer was limited to expansion of the intramuscular septa by collagen types I and III. The muscular arteries and veins within the strictured submucosa frequently exhibited eccentric, luminally oriented adventitial mantles comprising hyperplastic myocytes and extracellular type V collagen. We conclude that the fibromuscular remodeling which results in CD-associated ileal strictures predominantly involves the MM and submucosal vasculature in a luminally polarized fashion and suggests that mucosal-based factors may contribute to stricture pathogenesis.
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Authors
Xiaofei MD, PhD, Huaibin Mabel MD, Joana MD, Hinaben J. MS, Zhenjian MD, PhD, Mathilde MD, Bruce E. MD, Jean-Frederic MD, Judy MD, Bachir MD, Noam MD, PhD,