Autoimmune enteropathy
Jump to navigation
Jump to search
Autoimmune enteropathy, abbreviated AIE, is a rare gastrointestinal pathology.
General
- Considered a pediatric disease.
- Super rare in adults - there are only ~11 reported cases in the literature.[1]
- May be a component of the IPEX syndrome.[2]
Diagnosis is clinico-pathologic:[1]
- Intact immune system.
- Autoantibodies.
- Anti-enterocyte antibody.
- Anti-goblet antibody.
- Lack of response to gluten-free diet.
Microscopic
Features:[1]
- +/-Loss of goblet cells.
- +/-Loss of paneth cells.
- Villous blunting.
DDx:
See also
References
- ↑ 1.0 1.1 1.2 Akram, S.; Murray, JA.; Pardi, DS.; Alexander, GL.; Schaffner, JA.; Russo, PA.; Abraham, SC. (Nov 2007). "Adult autoimmune enteropathy: Mayo Clinic Rochester experience.". Clin Gastroenterol Hepatol 5 (11): 1282-90; quiz 1245. doi:10.1016/j.cgh.2007.05.013. PMC 2128725. PMID 17683994. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2128725/.
- ↑ Gentile, NM.; Murray, JA.; Pardi, DS. (Oct 2012). "Autoimmune enteropathy: a review and update of clinical management.". Curr Gastroenterol Rep 14 (5): 380-5. doi:10.1007/s11894-012-0276-2. PMID 22810979.