Autoimmune pancreatitis (AIP) is a rare entity in the paediatric population and its aetiology is unknown. Here, we report a 10-year-old girl with recurrent abdominal pain. A diagnosis of AIP was made based on elevated pancreatic enzymes, elevated IgG 4 and image findings. She responded to corticosteroid treatment. AIP should be considered in the differential diagnosis of recurrent pancreatitis. Correct diagnosis can help avert the consequences of progressive disease and unnecessary surgery.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963729 | PMC |
| http://dx.doi.org/10.7860/JCDR/2016/18437.7917 | DOI Listing |
Publication Analysis
Top Keywords
autoimmune pancreatitis
8
case report
4
report childhood
4
childhood recurrent
4
recurrent autoimmune
4
pancreatitis rare
4
rare emerging
4
emerging entity
4
entity autoimmune
4
pancreatitis aip
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!