Literature DB >> 8720659

Two forms of hereditary chronic pancreatitis.

H Sarles1, J Camarena, J P Bernard, J Sahel, R Laugier.   

Abstract

We report 11 families of hereditary pancreatitis characterized by the presence of calculi in pancreatic ducts. These were classified as (1) calcic lithiasis (one family with five cases), in which the calculi are composed of >95% calcium salts; and (2) protein lithiasis in 10 families, in which the calculi are composed of degraded amorphous residues of lithostathine, the pancreatic secretory protein that inhibits calcium salt crystallization. In both forms, transmission appears to be dominant. The average age at clinical onset of symptoms is 15 years. The clinical progression seems to be less severe than in alcoholic chronic pancreatitis (alcoholic calcic lithiasis). This report shows for the first time that hereditary chronic pancreatitis is a group of at least two diseases having a similar clinical picture and pathological features but different chemical compositions of calculi. This leads us to propose a revised Marseille-Rome classification.

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Year:  1996        PMID: 8720659     DOI: 10.1097/00006676-199603000-00005

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  2 in total

Review 1.  New insights into hereditary pancreatitis.

Authors:  D C Whitcomb
Journal:  Curr Gastroenterol Rep       Date:  1999-04

2.  Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis.

Authors:  I Nishimori; M Kamakura; K Fujikawa-Adachi; M Morita; S Onishi; K Yokoyama; I Makino; H Ishida; M Yamamoto; S Watanabe; M Ogawa
Journal:  Gut       Date:  1999-02       Impact factor: 23.059

  2 in total

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