scholarly journals Spontaneously Resolved Hepatic Artery Aneurysm Complicating A Laparoscopic Cholecystectomy

2021 ◽  
Vol 9 (3) ◽  
pp. 299-302
Author(s):  
  Y. El Badri ◽  
F. Adjimabou ◽  
B. Boutakioute ◽  
M. Ouali Idrissi ◽  
N. Cherif Idrissi Ganouni
2019 ◽  
Vol 3 (2) ◽  
Author(s):  
Al-Zayer FA ◽  
Alzahir MA ◽  
Abualsaud BA ◽  
Al-jaroof AH ◽  
Meshikhes AN

2021 ◽  
Vol 7 (2) ◽  
pp. 283-285
Author(s):  
Isabella Graham ◽  
John Kanitra ◽  
Richard Berg ◽  
Jimmy Haouilou

2020 ◽  
Vol 8 ◽  
pp. 232470962098243
Author(s):  
Khalid Sawalha ◽  
Anthony Kunnumpurath ◽  
Ronald McCann

An 80-year-old male patient presented with sepsis secondary to infected central line which was placed for native aortic valve endocarditis. He also had melena and abdominal pain prior to his presentation. Abdominal computed tomography (CT) was done, which showed cholelithiasis. Esophagogastroduodenoscopy was also done with no source of bleeding identified. Later, he developed hemodynamic instability requiring aggressive fluid resuscitation and multiple packed blood cell transfusions. In view of his hemodynamic instability, a repeat abdominal CT scan showed air droplets within the gallbladder pneumobilia, ascites, diverticulosis, and a bleeding infrahepatic hematoma measuring 6 × 10 cm, which was not on his prior scan 2 days prior. A mesenteric arteriogram was performed that identified an aneurysm of the right hepatic artery with no active bleeding; therefore, it was coiled. Due to his continued clinical decompensation, he underwent an urgent open cholecystectomy, in which serosanguineous fluid, cholecystocolic fistula, and old clot related to his previous bleed were encountered. However, control of bleeding was difficult, and the patient expired. We report this case of right hepatic artery aneurysm that we believe its etiology was related to eroding cholecystitis.


2017 ◽  
Vol 10 ◽  
pp. 117955221771143 ◽  
Author(s):  
Catherine Linzay ◽  
Abhishek Seth ◽  
Kunal Suryawala ◽  
Ankur Sheth ◽  
Moheb Boktor ◽  
...  

Background: Hepatic artery aneurysms (HAAs) constitute 14% to 20% of visceral artery aneurysms. Most HAAs are asymptomatic. Although rare, obstructive jaundice due to external bile duct compression or rupture of the HAA into the biliary tree with occlusion of the lumen from blood clots has been reported. Case presentation: A 56-year-old white man presented to an outside hospital with symptoms of obstructive jaundice, including abdominal pain and yellowing of the skin. Imaging showed a large HAA. Patient was transferred to our hospital where an endoscopic retrograde cholangiopancreatography with biliary stenting was performed. This was followed by coil embolization of the HAA with improvement in symptoms and liver chemistries. Conclusions: Most clinicians agree that management of HAA is highly variable and depends on clinical presentation and anatomic location. Biliary stenting provides temporary relief for patients with obstructive jaundice. Definitive options include open aneurysmal repair versus endovascular therapy. Hepatic artery aneurysms represent a significant risk for hemorrhage and therefore must be addressed promptly once discovered.


2003 ◽  
Vol 17 (2) ◽  
pp. 214-216 ◽  
Author(s):  
Mete Dolapci ◽  
Sadik Ersoz ◽  
Nuri A. Kama

2006 ◽  
Vol 58 (1) ◽  
pp. 9-12 ◽  
Author(s):  
Ioannis Tsitouridis ◽  
Konstantinos Tsinoglou ◽  
Christos Papastergiou ◽  
Christos Tsandiridis ◽  
Sofia Stratilati

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