کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3337590 1213807 2012 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Hemosuccus pancreaticus: a rare cause of gastroirtestiral bleeding
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کبدشناسی
پیش نمایش صفحه اول مقاله
Hemosuccus pancreaticus: a rare cause of gastroirtestiral bleeding
چکیده انگلیسی

BackgroundHemosuccus pancreaticus (HP) is defined as upper gastrointestinal (GI) hemorrhage from the papilla of Vater via the pancreatic duct and is a rare cause of digestive bleeding.Data SourceA PubMed search of relevant articles published from January 1967 to September 2011 was performed to identify current information about HP in terms of its etiology, pathophysiology, clinical presentation, diagnosis and management.ResultsA variety of etiological factors, most commonly chronic pancreatitis but also tumors and vascular diseases, can lead to this condition. Appropriate endoscopic or radiologic procedures should be chosen to establish a precise diagnosis for patients, especially those with a known history of pancreatic disorders, who present with abdominal pain, GI hemorrhage and hyperamylasemia. There are two main therapeutic options for this condition: angiographic embolotherapy and surgery. Both treatments can stop bleeding, but angiographic embolotherapy is the treatment of choice for stable patients. Recently, new and less invasive treatments have emerged to treat this condition.ConclusionsBecause of its rarity and broad spectrum of causes, HP is difficult to diagnose accurately. However, appropriate endoscopic and radiologic procedures are extremely helpful for establishing a correct diagnosis. Both angiographic embolotherapy and surgery are reliable treatment options for this condition, and transcatheter intervention is the treatment of choice for clinically stable patients. Additional innovative treatments have emerged, but their effectiveness and safety must be confirmed.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Hepatobiliary & Pancreatic Diseases International - Volume 11, Issue 5, October 2012, Pages 479-488