Abstract 17228: Not Just Another Knick In The Wall: An Unusual Case Of Multiple Arterial Aneurysms

Circulation ◽  
2021 ◽  
Vol 144 (Suppl_2) ◽  
Author(s):  
Vibha Amblihalli ◽  
Ayita Ray ◽  
Hafiz Khalid ◽  
luigi pacifico

Case Presentation: 47-year-old Liberian woman with a history of latent TB and no prior cardiac history presented with dyspnea, palpitations, and weight loss. She had fevers, tachycardia, and cervical lymphadenopathy. Cardiac exam showed widened pulse pressure, systolic and diastolic murmur, and features of heart failure. TTE showed dilated left ventricle with preserved ejection fraction, aortic root aneurysm compressing left atrium, severe aortic and mitral regurgitation, and moderate pericardial effusion with no tamponade. CT angiogram of neck, chest and abdomen showed right subclavian artery mycotic aneurysm, large left supraclavicular lymphadenopathy, multiple aortic arch, and descending thoracic aorta mycotic aneurysms. She underwent emergent surgical intervention. Intraoperative TEE revealed rupture of aortic root aneurysm into left ventricular outflow tract causing a fistula, perforated anterior mitral leaflet, and distortion of the left atrial wall. She underwent mitral and aortic tissue valve replacement, aortic root replacement, and a pericardial patch repair of the left atrial wall. Subsequently, she underwent right subclavian artery aneurysm resection, right carotid axillary bypass, and vertebral artery reimplantation. Aortic valve pathology was suggestive of endocarditis with negative cultures. Lymph node biopsy revealed non-necrotizing granulomatous inflammation with no evidence of acid-fast bacilli, fungi, and malignancy. Autoimmune workup was negative. A PET CT showed post-surgical inflammatory changes with no evidence of malignancy. Discussion: We describe an unusual case of multiple large arterial aneurysms causing severe valvular insufficiency requiring emergent surgical intervention. The patient underwent extensive workup which was unrevealing. She was treated for subacute bacterial endocarditis and suspected Bechet’s disease. Thus, the quest for a definitive diagnosis continues to elude us.

2015 ◽  
Vol 42 (2) ◽  
pp. 178-180 ◽  
Author(s):  
Marwan Saad ◽  
Ahmad Isbitan ◽  
Alaa Roushdy ◽  
Fayez Shamoon

Left atrial wall dissection is a rare condition; most cases are iatrogenic after mitral valve surgery. A few have been reported as sequelae of blunt chest trauma, acute myocardial infarction, and invasive cardiac procedures. On occasion, infective endocarditis causes left atrial wall dissection. We report a highly unusual case in which a 41-year-old man presented with native mitral valve infective endocarditis that had caused left atrial free-wall dissection. Although our patient died within an hour of presentation, we obtained what we consider to be a definitive diagnosis of a rare sequela, documented by transthoracic and transesophageal echocardiography.


Author(s):  
Satoshi Hayashida ◽  
Koichi Nagashima ◽  
Sayaka Kurokawa ◽  
Masaru Arai ◽  
Ryuta Watanabe ◽  
...  

2012 ◽  
Vol 93 (3) ◽  
pp. e57-e59 ◽  
Author(s):  
Giovanni Domenico Cresce ◽  
Diletta Peluso ◽  
Marco Panfili ◽  
Alessandro Favaro ◽  
Antonio Cannarella ◽  
...  

1990 ◽  
Vol 49 (3) ◽  
pp. 476-478 ◽  
Author(s):  
Kenneth S. Stone ◽  
John W. Brown ◽  
David Canal ◽  
Randy Caldwell ◽  
Roger Hurwitz ◽  
...  

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