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• W2092201943 abstract "Anti–tumor necrosis factor α (anti–TNF-α) therapy can result in endoscopic healing, reduction of symptoms, and reduced need for surgery and hospitalization in many patients with Crohn’s disease (CD). Earlier data suggested that anti–TNF-α therapy may be associated with fibrosis and stricturing. We sought to determine whether anti–TNF-α therapy affects histologic inflammation, fibrosis, and granuloma formation. Hematoxylin and eosin sections from 62 patients with CD treated with either infliximab or adalimumab and 80 controls undergoing the same surgery but without prior exposure to anti–TNF-α therapy were compared. All patients with CD had undergone surgery within 6 months of therapy; CD controls were matched for steroid exposure, procedure, and indication for surgery and were subcategorized and case matched. Blinded histologic assessment of all slides was performed using a semiquantitative scoring system to assess inflammatory changes and fibrosis in all bowel layers. Compared with controls, the group treated with anti–TNF-α showed a reduction in mucosal and submucosal inflammation (P < .05), a decrease in granuloma formation (P < .05), and an increase in duplication of the muscularis mucosae (P < .05). A notable feature was a distinct pattern of hyalinizing submucosal fibrosis that was often devoid of inflammatory cells and that started directly below the muscularis mucosae; this pattern was not observed in the control group (P < .05). Resection specimens from patients with CD treated with anti–TNF-α therapy showed (a) reduced mucosal and submucosal inflammation; (b) a decrease in granuloma formation; and (c) a distinct pattern of submucosal hyaline fibrosis, with increased fibrosis in the muscularis mucosae and muscularis propria." @default.
• W2092201943 created "2016-06-24" @default.
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• W2092201943 date "2014-09-01" @default.
• W2092201943 modified "2023-09-30" @default.
• W2092201943 title "Distinctive histopathologic phenotype in resection specimens from patients with Crohn’s disease receiving anti–TNF-α therapy" @default.
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• W2092201943 doi "https://doi.org/10.1016/j.humpath.2014.05.016" @default.
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