Pediatric Surgery International

, Volume 26, Issue 12, pp 1193–1199

Hereditary pancreatitis

Original Article

DOI: 10.1007/s00383-010-2684-4

Cite this article as:
Lal, A. & Lal, D.R. Pediatr Surg Int (2010) 26: 1193. doi:10.1007/s00383-010-2684-4


Hereditary chronic pancreatitis (HCP) is a rare disease in which chronic pancreatitis develops in childhood. HCP has autosomal dominant inheritance with approximately 80% penetrance. Diagnostic criteria are not universally agreed upon but the EUROPAC trial defined it as two first-degree relatives or at least 3 second-degree relatives in two or more generations, with chronic pancreatitis for which there is no other etiology. The gene for HCP was originally identified on chromosome 7 and subsequently many other genes have been reported to be associated with HCP. To date, no single genetic alteration has been found that is necessary for the development of HCP. In a recent study, 81% of patients with HCP were found to have a mutation of the PRSS1 gene. Patients with HCP are at risk for developing exocrine and endocrine insufficiency and there is a 50-fold increased risk of pancreatic cancer in HCP patients as compared with the general population.


Hereditary chronic pancreatitis Childhood pancreatitis Hereditary pancreatitis Chronic pancreatitis Familial pancreatitis 

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  1. 1.Department of SurgeryMedical College of WisconsinMilwaukeeUSA
  2. 2.Department of Pediatric Surgery, Children’s Research InstituteChildren’s Hospital of WisconsinMilwaukeeUSA