Prospective Evaluation of Subjects With Chronic Asymptomatic Pancreatic Hyperenzymemia.

Link to article at PubMed

Prospective Evaluation of Subjects With Chronic Asymptomatic Pancreatic Hyperenzymemia.

Am J Gastroenterol. 2012 May 15;

Authors: Amodio A, Manfredi R, Katsotourchi AM, Gabbrielli A, Benini L, Mucelli RP, Vantini I, Frulloni L

OBJECTIVES:Chronic asymptomatic pancreatic hyperenzymemia (CAPH) has been described since 1996 as a benign disease. Recent studies described pathological findings at magnetic resonance cholangiopancreatography with secretin stimulation (s-MRCP) in more than half of the CAPH subjects. The aim of this study was to investigate the frequency and clinical relevance of s-MRCP findings in patients with CAPH.METHODS:Subjects prospectively enrolled from January 2005 to December 2010 underwent s-MRCP and biochemical tests routinely performed.RESULTS:Data relative to 160 subjects (94 males, 66 females, age 49.6±13.6 years) were analyzed. In all, 51 (32%) subjects had hyperamylasemia, 9 (6%) hyperlipasemia, and 100 (62%) an increase in both enzyme levels. The time between the first increased dosage of serum pancreatic enzymes and our observation was 3.3±3.9 years (range: 1-15). Familial pancreatic hyperenzymemia was observed in 26 out of 133 subjects (19.5%). Anatomic abnormalities of the pancreatic duct system at s-MRCP were found in 24 out of 160 subjects (15%). Pathological MRCP findings were present in 44 subjects (27.5%) before and in 80 subjects (50%) after secretin administration (P<0.0001). Five subjects (3.1%) underwent surgery, 3 for pancreatic endocrine tumor, 1 for pancreatic adenocarcinoma, and 1 for intraductal papillary-mucinous neoplasia (IPMN) involving the main pancreatic duct, and 18 patients (11.3%) needed a follow-up (17 for IPMN and 1 for endocrine tumor).CONCLUSIONS:Alterations of the pancreatic duct system at s-MRCP in subjects with CAPH can be observed in 50% of the subjects and are clinically relevant in 14.4% of cases.Am J Gastroenterol advance online publication, 15 May 2012; doi:10.1038/ajg.2012.125.

PMID: 22584217 [PubMed - as supplied by publisher]

Leave a Reply

Your email address will not be published. Required fields are marked *