Celiac disease/Celiac sprue/Gluten sensitive enteropathy Clinical features, characteristic IEL distribution (villous tip heavy) serological screening (antibodies to tissue transglutaminase, gliadin ), response to gluten free diet (GFD), age >2years,exclusion of other possible cause
Refractory sprue Unresponsiveness to GFD, exclusion of other possible causes
Tropical sprue (TS) Mucosal changes in entire length of small intestine, Vitamin B12 and folate deficiency, response to tetracycline
Viral gastroenteritis Unresponsiveness to GFD, complete recovery with normal morphology
Parasitic infections like microsporidiosis, cyclosporidiosis, isosporiasis Usually seen in immunocompromised patients, demonstration of microorganism on the surface or within the enterocytes lining the villi
Autoimmune enteropathy Unresponsiveness to GFD, anti-enterocyte antibodies, response to steroids and immunosuppressive therapy
Crohn disease Focal acute inflammation flanked by normal appearing mucosa
Zollinger Ellison syndrome Concomitant gastric parietal cell hyperplasia
Enteropathy-type intestinal T cell lymphoma Multifocal monoclonal IELs affecting the entire small intestine.
Table 1: Differential diagnosis and salient features of conditions with intraepithelial lymphocytosis with partial/total villous architectural changes [4,5,8,9].