Ruptured Mycotic Abdominal Aortic Aneurysm in a Patient with Systemic Lupus Erythematosus

1998 ◽  
Vol 4 (1) ◽  
pp. 36-38
Author(s):  
Worawit Louthrenoo ◽  
Wannee Ojarasporn ◽  
Angkana Norasetthada ◽  
Waraporn Sukitawut
2000 ◽  
Vol 32 (1) ◽  
pp. 209-212 ◽  
Author(s):  
Naoki Washiyama ◽  
Teruhisa Kazui ◽  
Makoto Takinami ◽  
Katsushi Yamashita ◽  
Hitoshi Terada ◽  
...  

1999 ◽  
Vol 28 (3) ◽  
pp. 201-204
Author(s):  
Hitoshi Matsumoto ◽  
Toshiyuki Yuda ◽  
Takayuki Ueno ◽  
Yousuke Hisashi ◽  
Yukinori Moriyama ◽  
...  

1994 ◽  
Vol 23 (3) ◽  
pp. 217-220 ◽  
Author(s):  
Toshihiko Shibata ◽  
Tadashi Yamada ◽  
Kanji Ishihara ◽  
Norio Suzuki ◽  
Masataka Eirai ◽  
...  

Author(s):  
Kensuke Kobayashi ◽  
Nobuyuki Inoue ◽  
Takuma Fukunishi

Abstract Mycotic abdominal aortic aneurysms are rare but life-threatening, and no standard therapy has yet been established. Effective surgery with intensive antimicrobial therapy is crucial; however, this can be fatal in immunocompromised patients. Only a few reports of mycotic abdominal aortic aneurysm with concomitant autoimmune disease exist; therefore, we were concerned about our lack of experience and knowledge about appropriate treatment. We report a 69-year-old male with a mycotic abdominal aortic aneurysm secondary to septic shock after spinal fusion surgery. He had also been on long-term oral immunosuppressants for systemic lupus erythematosus. After preoperative cephazolin, we performed debridement of infected tissue, graft replacement with a rifampicin-bonded prosthesis, and omentopexy. On the 52nd postoperative day, he was transferred back to the previous attending hospital under oral antibiotics and prednisolone. Mycotic abdominal aortic aneurysm in patients with systemic lupus erythematosus should be treated with in situ replacement using an antimicrobial prosthetic or biological graft with thorough debridement and omentopexy, followed by antimicrobials and immunosuppressants, as needed.


2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
David Noorvash ◽  
Kevin King ◽  
Meera Gebrael

We present two cases of young women with a past medical history significant for systemic lupus erythematosus (SLE), who presented to the Emergency Department with a ruptured abdominal aortic aneurysm (AAA). These cases are of particular interest because the patients did not fit the typical demographic for patients who present with a ruptured AAA. Based on these cases and a review of the relevant literature, ED providers should maintain a higher index of suspicion for AAA rupture in patients with autoimmune diseases, especially SLE.


2019 ◽  
Vol 2019 ◽  
pp. 1-5 ◽  
Author(s):  
Valerie R. Ramiro ◽  
Carmegie C. Saliba ◽  
John Anthony D. Tindoc ◽  
Marinette R. Jambaro ◽  
Enrique M. Chua ◽  
...  

Aortic aneurysms are not commonly reported among patients with systemic lupus erythematosus (SLE). We report a case of a 47-year-old Filipino female diagnosed with SLE 17 years ago maintained on prolonged oral steroids, azathioprine, and hydroxychloroquine. She also had lupus nephritis, secondary hypertension, and dyslipidemia. She initially presented with a week-long watery nonbloody diarrhea with associated diffuse crampy abdominal pain and generalized weakness. She was admitted for a week at a provincial hospital and was given an unrecalled antibiotic with resolution of symptoms. Upon discharge, however, she experienced two weeks of severe right lower quadrant pain radiating to the back and left lower quadrant, with no history of diarrhea, vomiting, dysuria, and fever. Complete blood count showed slight leukocytosis and elevated C-reactive protein. Abdominal imaging revealed a saccular infrarenal aneurysm with dissection. An atherosclerotic mechanism was primarily considered, but a vasculitic process was likewise considered due to elevated acute phase reactants. The initial plan was Endovascular Aneurysm Repair (EVAR) but due to financial limitations, an exploratory laparotomy with infrarenal endoaneurysmorrhaphy was eventually performed. Intraoperative findings were a saccular infrarenal aneurysm with dissection up to the proximal right common iliac artery and an abscess compartment within the false lumen in the anterior aortic wall. Abscess culture yielded high growth of Salmonella group B. Micrographs of the aortic wall biopsy showed fibrin deposition necrosis and calcification with peripheral viable cellular infiltrates consisting of neutrophils and foamy macrophages. Inadvertently placing an endovascular graft in an infected aortic aneurysm would have led to graft infection and catastrophic morbidity. We highlight the significance of having a high index of suspicion for infectious causes of aortitis among immunocompromised patients presenting with aneurysm prior to pursuing an endovascular versus an open approach for repair.


2010 ◽  
Vol 49 (20) ◽  
pp. 2263-2266 ◽  
Author(s):  
Tomoko Miyashita ◽  
Yukio Abe ◽  
Yasuyuki Kato ◽  
Eiichiro Nakagawa ◽  
Ryushi Komatsu ◽  
...  

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