Hemosuccus Pancreaticus due to Intraductal Pseudoaneurysm
نویسندگان
چکیده
منابع مشابه
Hemosuccus Pancreaticus Due to Rupture of a Gastroduodenal Artery Pseudoaneurysm
Hospital Physician September 2007 61 H emorrhage from the pancreatic duct, referred to as hemosuccus pancreaticus or pseudohemobilia, is a rare cause of gastrointestinal (GI) bleeding. This potentially life-threatening complication of pancreatitis may pose a significant diagnostic and therapeutic dilemma, especially in patients who do not exhibit symptoms such as abdominal pain, jaundice, or GI...
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Introduction: Hemosuccus pancreaticus is a rare cause of gastrointestinal bleeding due to hemorrhage into the pancreatic duct, most commonly from pseudoaneurysms. Due to its rarity as well as the intermittent nature of the bleeding, diagnosis is commonly delayed. We report an interesting case of hemosuccus pancreaticus and the associated management issues. Case Report: We report a 32 year old m...
متن کاملHemosuccus pancreaticus due to a noninflammatory pancreatic pseudotumor.
CONTEXT Hemosuccus pancreaticus is a rare source of gastrointestinal bleeding, the most frequent cause of which is pancreatitis, followed by tumors, but nearly all these tumors are true neoplasms, and not pseudotumors. Furthermore, nearly all pseudotumors of the pancreas and retroperitoneum are inflammatory. CASE REPORT We present a case of hemosuccus pancreaticus associated with a nonneoplas...
متن کاملHemosuccus Pancreaticus: A Rare Entity
Hemosuccus pancreaticus, also named as Wirsungorrhagia or psuedohematobilia is a rare condition of intermittent hemorrhage from upper gastrointestinal tract. The source of bleeding is from a visceral aneurysm into main pancreatic duct in patients with chronic pancreatitis. It is a life threatening complication of pancreatitis and a significant diagnostic challenge due to its intermittent nature...
متن کاملHemophilia A Presenting as Hemosuccus Pancreaticus
Hemosuccus pancreaticus (HP) is a rare cause of upper gastrointestinal bleeding. Case of haemophilia A presenting as HP has not been reported. We describe the case of a 50 year old patient, who presented with complaints of melena, he was initially diagnosed as HP on upper gastrointestinal (GI) endoscopy and following extensive workup patient also diagnosed with mild hemophilia A. Factor VIII in...
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ژورنال
عنوان ژورنال: Korean Journal of Pancreas and Biliary Tract
سال: 2016
ISSN: 2288-0941
DOI: 10.15279/kpba.2016.21.1.40