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Adult-onset autoimmune-type enteropathy: potential relationship to an adverse drug reaction

OBJECTIVE: To describe an example of adult-onset autoimmune enteropathy (AIE) that coincided with drug-induced reaction. DESIGN: A 54-year-old patient was presented with Stevens-Johnson syndrome after a course of quinolones. This was followed shortly thereafter by epigastric pain, diarrhoea and weig...

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Detalles Bibliográficos
Autores principales: Chetty, Runjan, Cino, Maria, Okrainec, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904145/
https://www.ncbi.nlm.nih.gov/pubmed/31875138
http://dx.doi.org/10.1136/bmjgast-2019-000319
Descripción
Sumario:OBJECTIVE: To describe an example of adult-onset autoimmune enteropathy (AIE) that coincided with drug-induced reaction. DESIGN: A 54-year-old patient was presented with Stevens-Johnson syndrome after a course of quinolones. This was followed shortly thereafter by epigastric pain, diarrhoea and weight loss. She also developed an autoimmune neutropenia. RESULTS: Several biopsies were performed from the upper and lower gastrointestinal tract (GIT). The duodenal biopsies showed intraepithelial lymphocytosis; therefore, coeliac disease was considered. However, confirmatory serology was negative and the patient did not respond to a gluten-free/gliadin-free diet. Both upper and lower GIT biopsies consistently showed an absence of goblet cells resembling the changes of an AIE. CONCLUSION: This is an unusual case of autoimmune-pattern enteropathy in an adult that was potentially drug-induced.