Hereditær pankreatitis

Ming Tan; Ove B. Schaffalitzky; Maiken Thyregod Jørgensen

Hereditær pankreatitis

Ming Tan^*, Ove B. Schaffalitzky, Maiken Thyregod Jørgensen

^*Kontaktforfatter

KI, OUH, Forskningsenhed for Medicinsk gastroenterologi (Odense)

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Abstract

Hereditary pancreatitis (HP) is an autosomal dominant disease with 80% penetrance. HP is characterised by the debut of recurrent acute pancreatitis episodes during childhood with gradual progression to chronic pancreatitis. Patients with phenotypic HP have a significantly increased lifetime risk of developing pancreatic ductal adenocarcinoma (PDAC). Patients with HP represent a rare but important group of high-risk individuals in need of early diagnosis and screening for potential PDAC. The aim of this review is to provide an overview of the epidemiology, genetics and clinical aspects of HP.

Bidragets oversatte titel	Hereditary pancreatitis
Originalsprog	Dansk
Artikelnummer	V11190676
Tidsskrift	Ugeskrift for Læger
Vol/bind	182
Udgave nummer	18
Sider (fra-til)	1684-1686
ISSN	0041-5782
Status	Udgivet - 14. sep. 2020

Dokumenter og links

https://ugeskriftet.dk/videnskab/hereditaer-pankreatitis

Citationsformater

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T1 - Hereditær pankreatitis

AU - Tan, Ming

AU - Schaffalitzky, Ove B.

AU - Jørgensen, Maiken Thyregod

PY - 2020/9/14

Y1 - 2020/9/14

N2 - Hereditary pancreatitis (HP) is an autosomal dominant disease with 80% penetrance. HP is characterised by the debut of recurrent acute pancreatitis episodes during childhood with gradual progression to chronic pancreatitis. Patients with phenotypic HP have a significantly increased lifetime risk of developing pancreatic ductal adenocarcinoma (PDAC). Patients with HP represent a rare but important group of high-risk individuals in need of early diagnosis and screening for potential PDAC. The aim of this review is to provide an overview of the epidemiology, genetics and clinical aspects of HP.

AB - Hereditary pancreatitis (HP) is an autosomal dominant disease with 80% penetrance. HP is characterised by the debut of recurrent acute pancreatitis episodes during childhood with gradual progression to chronic pancreatitis. Patients with phenotypic HP have a significantly increased lifetime risk of developing pancreatic ductal adenocarcinoma (PDAC). Patients with HP represent a rare but important group of high-risk individuals in need of early diagnosis and screening for potential PDAC. The aim of this review is to provide an overview of the epidemiology, genetics and clinical aspects of HP.

M3 - Tidsskriftartikel

SN - 0041-5782

VL - 182

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EP - 1686

JO - Ugeskrift for Læger

JF - Ugeskrift for Læger

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Hereditær pankreatitis

Abstract

Dokumenter og links

Fingeraftryk

Citationsformater