TY - JOUR
T1 - Hemosuccus pancreaticus as an unusual cause of upper gastrointestinal bleeding
T2 - Case report and literature review
AU - Ayala, Daniela
AU - González T, Juliana
AU - Pedroza, Felipe
AU - Rey Chaves, Carlos Eduardo
AU - Conde, Danny
AU - Sabogal Olarte, Juan Carlos
N1 - Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
Publisher Copyright:
© 2022 The Authors
PY - 2022/10
Y1 - 2022/10
N2 - BACKGROUND: Hemosuccus pancreaticus is a rare cause of upper gastrointestinal bleeding (1/1500) and represents the loss of blood through the main pancreatic duct and its exteriorization through the major duodenal papilla. It can lead to massive bleeding, which is potentially life-threatening. This condition most commonly follows pseudoaneurysm formation due to acute or chronic pancreatitis. As a result of its infrequency, it is difficult to diagnose, and the mortality rate remains high. To our knowledge, this is the first case report on the Latin-American population.CASE PRESENTATION: A 70-year-old male patient presented with diffuse severe abdominal pain associated with melaena. Angiotomography was performed, ruling out mesenteric ischemia, with evidence of pancreatic head tumor with liver metastases. Sandblom's triad was present and the diagnosis of hemosuccus pancreaticus was confirmed. Multiple arteriograms were performed, with pseudoaneurysm of gastroduodenal artery findings. Therefore, endovascular coil embolization was performed in two opportunities to control the bleeding.CONCLUSION: Upper gastrointestinal bleeding is a clinical challenge for the surgeon and emergency medicine. It's a complex entity with high mortality that should be suspected in patients with acute or chronic pancreatitis and periampullary tumors with non-established sources of bleeding. Clinically manifested by Sandblom's triad. Its diagnosis gold standard is arteriography plus embolization which is also therapeutic. Surgery is related to higher mortality and reserved for specific situations.
AB - BACKGROUND: Hemosuccus pancreaticus is a rare cause of upper gastrointestinal bleeding (1/1500) and represents the loss of blood through the main pancreatic duct and its exteriorization through the major duodenal papilla. It can lead to massive bleeding, which is potentially life-threatening. This condition most commonly follows pseudoaneurysm formation due to acute or chronic pancreatitis. As a result of its infrequency, it is difficult to diagnose, and the mortality rate remains high. To our knowledge, this is the first case report on the Latin-American population.CASE PRESENTATION: A 70-year-old male patient presented with diffuse severe abdominal pain associated with melaena. Angiotomography was performed, ruling out mesenteric ischemia, with evidence of pancreatic head tumor with liver metastases. Sandblom's triad was present and the diagnosis of hemosuccus pancreaticus was confirmed. Multiple arteriograms were performed, with pseudoaneurysm of gastroduodenal artery findings. Therefore, endovascular coil embolization was performed in two opportunities to control the bleeding.CONCLUSION: Upper gastrointestinal bleeding is a clinical challenge for the surgeon and emergency medicine. It's a complex entity with high mortality that should be suspected in patients with acute or chronic pancreatitis and periampullary tumors with non-established sources of bleeding. Clinically manifested by Sandblom's triad. Its diagnosis gold standard is arteriography plus embolization which is also therapeutic. Surgery is related to higher mortality and reserved for specific situations.
KW - Angiographic embolization
KW - Hemoductal pancreatitis
KW - Hemosuccus pancreaticus
KW - Pseudohemobilia
KW - Upper gastrointestinal bleeding
KW - Wirsungrhagia
UR - http://www.scopus.com/inward/record.url?scp=85137724841&partnerID=8YFLogxK
U2 - 10.1016/j.ijscr.2022.107624
DO - 10.1016/j.ijscr.2022.107624
M3 - Artículo
C2 - 36113372
SN - 2210-2612
VL - 99
SP - 107624
JO - International Journal of Surgery Case Reports
JF - International Journal of Surgery Case Reports
M1 - 107624
ER -