Hasosah Mohammed Y, Masawa Lojain, Jan Ajwan, Alsaleem Khalid
Assistant Professor, Department of Pediatric Gastroenterology, King Saud Bin Abdulaziz University for Health Sciences, National Guard Hospital , Jeddah, Saudi Arabia .
Paediatric Intern, Department of Pediatrics, King Saud Bin Abdulaziz University for Health Sciences, National Guard Hospital , Jeddah, Saudi Arabia .
J Clin Diagn Res. 2016 Jun;10(6):SD01-2. doi: 10.7860/JCDR/2016/18437.7917. Epub 2016 Jun 1.
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.
自身免疫性胰腺炎(AIP)在儿科人群中是一种罕见疾病,其病因尚不清楚。在此,我们报告一名10岁反复腹痛的女孩。根据胰腺酶升高、IgG 4升高及影像学表现诊断为AIP。她对皮质类固醇治疗有反应。在复发性胰腺炎的鉴别诊断中应考虑AIP。正确诊断有助于避免疾病进展和不必要手术的后果。