scholarly journals S2347 Spontaneous Ruptured Splenic Artery Aneurysm Presenting as an Acute Abdominal Mass

2021 ◽  
Vol 116 (1) ◽  
pp. S998-S999
Author(s):  
Zeinab Abdulrahman ◽  
M'hamed Turki ◽  
Hayder Azeez ◽  
Abdelhamid Ben Selma
2015 ◽  
Vol 143 (5-6) ◽  
pp. 326-331 ◽  
Author(s):  
Sinisa Pejkic ◽  
Ivan Tomic ◽  
Dragan Opacic ◽  
Luka Pejinovic ◽  
Nikica Grubor ◽  
...  

Introduction. Splenic artery aneurysms are potentially lethal lesions. We report two illustrative cases and discuss etiology, diagnosis and treatment of these aneurysms. Outline of Cases. Both patients, age 31 and 80 years, were biparous women. The younger woman, otherwise healthy, was referred from a local hospital 3 weeks after she underwent a left subcostal laparotomy and exploration for symptomatic abdominal mass diagnosed by CT. Angiography established the diagnosis of a large, non-ruptured splenic artery aneurysm. Elective aneurysmectomy with splenectomy was performed using the approach through the upper median laparotomy and bursa omentalis. Postoperative course was uneventful. Histopathology demonstrated cystic medial necrosis with chronic dissection. The other patient, elderly woman, presented urgently with acute abdominal pain and syncope and was diagnosed by computed tomography with a huge, ruptured splenic artery aneurysm. She underwent immediate aneurysmectomy with splenectomy using the same, above-mentioned approach. External pancreatic fistula and pancreatic pseudocyst complicated the postoperative course, requiring open pseudocyst drainage and cystojejunostomy. After a protracted hospitalization patient eventually recovered. The pathological diagnosis was atherosclerotic aneurysm. Conclusion. Splenic artery aneurysms are infrequent lesions, with varied etiology and clinical presentation. Timely diagnosis and adequate treatment prevent life-threatening rupture and lessen the risk of operative morbidity and mortality.


2002 ◽  
Vol 95 (9) ◽  
pp. 460-461 ◽  
Author(s):  
R Kenningham ◽  
M J Hershman ◽  
R G Mcwilliams ◽  
F Campbell

2019 ◽  
Vol 89 (2) ◽  
Author(s):  
Cuneyt Tetikkurt ◽  
Zeynep Ferhan Ozseker ◽  
Fatma Gülsüm Karakaş

A 40-year-old female presented with cough, exertional dyspnea, abdominal pain with distention, fatigue, dry eyes and dry mouth. Past history revealed asthma. Physical examination was normal except for tachypnea. We found leukocytosis, azygos fissure on chest X-ray along with normal pulmonary function tests and arterial blood gases.  Thorax computed tomography (CT) revealed bronchiectasis and ground glass opacities in both lungs. Abdominal CT demonstrated thrombosed proximal splenic artery aneurysm. Further diagnostic procedures were done and according to the positive Schirmer test and compatible histopathologic findings of the salivary gland, diagnosis of primary Sjögren’s syndrome was established. Splenic artery aneurysm is rare occurring in less than 1% of the population that usually appears as an incidental finding. This is the first case in literature that introduces Sjögren’s syndrome as a risk factor for splenic artery aneurysm. The silent presentation of the splenic artery aneurysm should previse the clinicians that such an occurrence may cause a significant diagnostic dilemma.


2001 ◽  
Vol 24 (3) ◽  
pp. 200-203 ◽  
Author(s):  
Hyun-Ki Yoon ◽  
Mats Lindh ◽  
Petr Uher ◽  
Bengt Lindblad ◽  
Krasnodar Ivancev

2003 ◽  
Vol 73 (5) ◽  
pp. 361-364 ◽  
Author(s):  
Eugene T. Ek ◽  
Carol-Anne Moulton ◽  
Sean Mackay

EJVES Extra ◽  
2003 ◽  
Vol 6 (3) ◽  
pp. 62-63 ◽  
Author(s):  
D. Kasir ◽  
J. Macierewicz ◽  
M. Castillo-Rama ◽  
S. Singh ◽  
J. Mackinlay

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