Pancreatic involvement in cystic fibrosis

dc.authorscopusid35562819000
dc.contributor.authorSelimo?lu M.A.
dc.date.accessioned2024-08-04T20:02:35Z
dc.date.available2024-08-04T20:02:35Z
dc.date.issued2011
dc.departmentİnönü Üniversitesien_US
dc.description.abstractCystic fibrosis (CF) is an autosomal genetic disease causing an accumulation of mucus in many exocrine organs. It is the most frequent cause of exocrine pancreatic insufficiency in childhood. Approximately 85 to 90% of CF patients are pancreatic insufficient (PI), however, there is an increase in the number of CF patients who are pancreatic sufficient (PS). Other than PS and PI groups, an additional third group including PS patients with late conversion from PS to PI has been described. Although there are several ways to determine that conversion, faecal elastase-1 is the ideal marker of endogenous pancreatic secretion. Recurrent acute and chronic pancreatitis is not rare in PS individuals; pancreatitis may be the presenting symptom. In cases with PI, there is a minimal risk of inflammatory or neoplastic changes, whereas a functioning pancreas is at risk of developing pancreatitis. Few cases of pancreatic cancer are reported in CF patients, but overall risk is unknown. Patients with malabsorption should receive pancreatic enzyme replacement, however, if gastrointestinal symptoms and signs are absent or minimal, definitive evidence of malabsorption should first be identified. © Touch Briefings 2011.en_US
dc.identifier.endpage53en_US
dc.identifier.issn1758-3799
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-79954617300en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage51en_US
dc.identifier.urihttps://hdl.handle.net/11616/91804
dc.identifier.volume7en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTouch Briefingsen_US
dc.relation.ispartofEuropean Gastroenterology and Hepatology Reviewen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCystic fibrosisen_US
dc.subjectPancreasen_US
dc.titlePancreatic involvement in cystic fibrosisen_US
dc.typeArticleen_US

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