Agenesis of the dorsal pancreas
Agenesis of the dorsal pancreas作者机构:Practice for General Internal MedicineHauptstrasse 5A-8940 LiezenAustria Department of Internal MedicineMedical UniversityAuenbruggerplatz 15A-8036 GrazAustria Institute of PathophysiologyCenter for Molecular MedicineHeinrichstrasse 31aA-8010 GrazAustria
出 版 物:《World Journal of Gastroenterology》 (世界胃肠病学杂志(英文版))
年 卷 期:2009年第15卷第3期
页 面:376-377页
核心收录:
学科分类:1002[医学-临床医学] 100210[医学-外科学(含:普外、骨外、泌尿外、胸心外、神外、整形、烧伤、野战外)] 10[医学]
基 金:Author contributions: Schnedl WJ Lipp RW gave the conception and designed the letter Sebnedl WJ Piswanger-Soelkner C analyzed and interpreted the data Schnedl WJ drafted and critically revised the article for important intellectual content Schnedl W J Wallner S J Lipp RW finally approved the article Schnedl WJ Piswanger-Soelkner C Wallner S J Krause R Lipp RW gave the administrative technical or logistic support Wallner S J Krause R Lipp RW collected and assembled the data
主 题:Agenesis of dorsal pancreas Diabetesmellitus Glucose intolerance Abdominal pain Pancreatitis
摘 要:During the last 100 years in medical literature,there are only 54 reports,including the report of Pasaoglu et al(World J Gastroenterol 2008;14:2915-2916),with clinical descriptions of agenesis of the dorsal pancreas in *** of the dorsal pancreas,a rare congenital pancreatic malformation,is associated with some other medical conditions such as hyperglycemia,abdominal pain,pancreatitis and a few other *** approximately 50% of reported patients with this congenital malformation,hyperglycemia was *** of hyperglycemia and diabetes mellitus in all patients with agenesis of the dorsal pancreas including description of fasting blood glucose,oral glucose tolerance test,glycated hemoglobin and medical treatment would be a future *** autosomal dominant transmission has been suggested in single families,more family studies including imaging technologies with demonstration of the pancreatic duct system are needed for evaluation of this *** this letter to the editor,we aim to increase available information for the better understanding of this rare disease.