| Literature DB >> 22691596 |
Rebecca Thompson1, Vijayalakshmi Kothandaraman.
Abstract
A 5-year-old male presented with a 1-day history of vomiting, epigastric pain, loose stools and poor oral intake. The child had intermittent symptoms of abdominal pain and vomiting for the past 2 years and there was a strong family history of chronic hereditary pancreatitis. A random serum amylase was elevated at 2320 IU/l. Abdominal ultrasound scan revealed no abnormalities. On the basis of the family history, positive symptoms and elevated amylase, a diagnosis of hereditary pancreatitis was made. The child received symptomatic management and treatment for his acute illness. He is currently awaiting results from molecular testing.Entities:
Mesh:
Year: 2011 PMID: 22691596 PMCID: PMC3116219 DOI: 10.1136/bcr.12.2010.3560
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X