scholarly journals A CASE OF SPLENIC ARTERY ANEURYSM ANOMALOUSLY ORIGINATING FROM THE SUPERIOR MESENTERIC ARTERY

2000 ◽  
Vol 61 (5) ◽  
pp. 1275-1278
Author(s):  
Takahiro MANABE ◽  
Tomishige AMANO ◽  
Kiyotaka IMOTO ◽  
Shin-ichi SUZUKI ◽  
Jiro KONDO ◽  
...  
Vascular ◽  
2013 ◽  
Vol 21 (2) ◽  
pp. 105-108 ◽  
Author(s):  
Sydney S N Wong ◽  
T F Lindsay ◽  
G Roche-Nagle

Aneurysms of the splenic artery are the most common visceral aneurysm. A splenomesenteric trunk, which involves the splenic artery arising from the superior mesenteric artery (SMA), is rare and occurs in less than 1% of patients. Thus splenic artery aneurysms (SAAs) with an anomalous origin from the SMA are quite rare. We report our experience with the surgical management of a 2.6-cm aneurysm involving a splenic artery arising from the SMA in a 40-year-old woman. This was treated with surgical resection with preservation of the spleen. A discussion about SAAs and the management of aneurysms arising from a splenomesenteric trunk follows.


2017 ◽  
Vol 51 (3) ◽  
pp. 152-154 ◽  
Author(s):  
Lalithapriya Jayakumar ◽  
Francis J. Caputo ◽  
Joseph V. Lombardi

A 22 year old female with a history of recurrent abdominal pain was transferred to our institution with a diagnosis of splenic artery aneurysm identified on imaging. CT angiography of the abdomen and pelvis revealed a partially thrombosed 3.0 cm splenic artery aneurysm without signs of rupture and with an anomalous origin from the superior mesenteric artery. The patient was successfully treated with endovascular exclusion of the aneurysm. Herein we review some of the nuances of endovascular repair of splenic artery aneurysm.


2021 ◽  
pp. 1-4
Author(s):  
Reham Almasoud ◽  
Alaaeddin Nwilati ◽  
Saeb Bayazid ◽  
Mamoun Shafaamri

We herein report a rare case of mycotic aneurysm of the superior mesenteric artery caused by <i>Klebsiella pneumoniae</i>. A 66-year-old man, a known case of hypertension and aorto-oesophageal fistula with stented aorta in 2010 and 2018, presented to the emergency department multiple times over 2 months with severe postprandial abdominal pain associated with vomiting and fever. On his last presentation, the obtained blood cultures grew ESBL positive <i>K. pneumoniae</i> and a repeated computed tomography (CT) showed a growing aneurysm at the origin of the ileocecal branch of the superior mesenteric artery measuring 17 × 10 mm (the aneurysm was 8 × 7.5 mm in the CT angiography on the previous admission). Extensive workup did not reveal the underlying cause of the mycotic aneurysm, thus we believe the cause to be the infected aortic stent, leading to bacteraemia and vegetations to the mesenteric artery causing the aneurysm. The management plan was placed by a multidisciplinary team consisting of vascular surgeons and infectious disease specialists along with review from a dietician to evaluate the patient’s nutritional status. The patient was started on total parenteral nutrition due to his postprandial pain and on antibiotic therapy according to the infectious disease team’s recommendation. He underwent surgical resection of the mycotic aneurysm, which showed a thrombosed aneurysm in the jejunoileal mesenteric area. The histopathology of the resected tissue demonstrated inflammatory aneurysm of the mesenteric artery. Following the surgery, the patient continued his antibiotic therapy and was discharged on the 13th post-operative day with follow-up appointments in the vascular surgery and infectious disease clinic.


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

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