HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Pathology analysis reveals that dysplastic pancreatic ductal lesions are frequent in patients with hereditary pancreatitis.

AbstractBACKGROUND & AIMS:
Hereditary pancreatitis (HP) is a risk factor for pancreatic adenocarcinoma. We performed a retrospective, multicenter study to characterize and evaluate the frequency of pancreatic intraepithelial neoplasia (PanIN) and to describe the characteristics of fibrosis in pancreatic surgical specimens from patients with HP.
METHODS:
Samples from partial pancreatectomies (n = 13) of patients with HP complications (n = 12; 7 males; mean age, 24 y; 1 patient underwent 2 surgeries over 16 years) were analyzed by histologic and immunohistologic analyses; patients with suspected or proven pancreatic adenocarcinoma were excluded. HP diagnosis was confirmed by analysis of PRSS1 mutations. Dysplastic lesions were described according to the PanIN classification.
RESULTS:
Eleven patients were found to have the R122H mutation in PRSS1 and 1 patient was found to have the N29I mutation in PRSS1. Fifty-one PanIN lesions were observed in 10 specimens (77%): PanIN lesions 1a, 1b, 2, and 3 were observed in 8, 5, 8, and 5 specimens, respectively. The median number of PanIN lesions was 3.5 for each specimen. The density of the lesions was 2.6 per 10 cm(2). The size of lesions was greater than 0.5 mm in 55% of the samples. Two patients with PanIN-3 developed pancreatic cancer, 18 months and 44 years after surgery.
CONCLUSIONS:
PanIN lesions are frequent, severe, and occur early in the course of HP. Among patients with PanINs, 50% had PanIN-3 lesions. Pancreatectomy could be considered as a prophylactic against pancreatic cancer in patients with high-grade dysplasia.
AuthorsVinciane Rebours, Philippe Lévy, Jean-François Mosnier, Jean-Yves Scoazec, Marie-Sophie Soubeyrand, Jean-François Fléjou, Bruno Turlin, Pascal Hammel, Philippe Ruszniewski, Pierre Bedossa, Anne Couvelard
JournalClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association (Clin Gastroenterol Hepatol) Vol. 8 Issue 2 Pg. 206-12 (Feb 2010) ISSN: 1542-7714 [Electronic] United States
PMID19765677 (Publication Type: Journal Article, Multicenter Study)
CopyrightCopyright 2010 AGA Institute. Published by Elsevier Inc. All rights reserved.
Chemical References
  • PRSS1 protein, human
  • Trypsin
Topics
  • Adolescent
  • Adult
  • Carcinoma in Situ (epidemiology)
  • Carcinoma, Pancreatic Ductal (epidemiology)
  • Child
  • Child, Preschool
  • Female
  • Genetic Diseases, Inborn (complications)
  • Humans
  • Male
  • Middle Aged
  • Pancreatectomy
  • Pancreatic Ducts (pathology)
  • Pancreatic Neoplasms (epidemiology)
  • Pancreatitis (complications)
  • Retrospective Studies
  • Trypsin (genetics)
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: