scholarly journals Left ventricular aneurysm in Behçet's disease

2008 ◽  
Vol 101 (5) ◽  
pp. 375 ◽  
Author(s):  
Gérard Helft ◽  
Claude Le Feuvre ◽  
Bertrand Wechsler
1991 ◽  
Vol 51 (1) ◽  
pp. 131-132 ◽  
Author(s):  
G. Di Eusanio ◽  
A. Mazzola ◽  
R. Gregorini ◽  
G. Esposito ◽  
W. Di Nardo ◽  
...  

BMC Surgery ◽  
2005 ◽  
Vol 5 (1) ◽  
Author(s):  
Seyed Mojtaba Marashi ◽  
Payam Eghtesadi-Araghi ◽  
Mohammad Hussein Mandegar

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Miklós Pólos ◽  
Ádám Koppányi ◽  
Kálmán Benke ◽  
László Daróczi ◽  
Attila Oláh ◽  
...  

Abstract Background Behçet’s disease is an auto-inflammatory disorder categorized as a primer systemic vasculitis of unknown aetiology. Genetic factors, infectious agents and the irregularity of T-cell homeostasis are presumed to be responsible for the emergence of Behçet’s disease. Characteristic symptoms are multisystemic. Although cardiovascular involvement is rare, it should be noted due to the difficulty of surgical treatment options. Case presentation Our 44-year-old male patient underwent aortic valve replacement due to aortic regurgitation. At the 15-month follow-up, echocardiography showed detachment of the prosthetic valve and in the aortic root, multiple pseudo-aneurysms were identified. We performed an aortic root reconstruction with a Bentall procedure using a special „skirted” conduit to reduce strain in the suture line between the conduit and the extremely dilated left ventricular outflow tract. Conclusions The surgical treatment of cardiovascular manifestations of Behçet’s disease remains challenging. This new technique may be beneficial in well-selected cases where the annulus of the aorta is extremely dilated or annular tissue disorder is present.


1990 ◽  
Vol 11 (10) ◽  
pp. 957-959 ◽  
Author(s):  
G. VANHALEWEYK ◽  
K. M. EL-RAMAHI ◽  
M. HAZMI ◽  
J. O. SIECK ◽  
L. ZAMAN ◽  
...  

2010 ◽  
Vol 140 ◽  
pp. S6
Author(s):  
Tolga Aksu ◽  
Erdem Guler ◽  
Mine Kosar ◽  
Nurcan Arat ◽  
Omac Tufekcioglu ◽  
...  

2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 1082.1-1083
Author(s):  
A. A. Ahmed ◽  
S. Tharwat ◽  
N. M. Batouty ◽  
S. D. Abd El-Halim

Background:Behçet’s disease is a multisystemic vasculitis characterized by mucocutaneous, ocular, arthritic, and vascular manifestations.[1] However, the incidence and nature of cardiac involvement in Behcet’s disease have not been clearly documented yet.Objectives:This study aimed to assess the cardiac involvement in patients with Behçet’s disease using cardiac magnetic resonance imaging (MRI).Methods:This cross -sectional descriptive study was carried out on thirty consecutive patients with Behçet’s disease (21 males,9 females) with mean age 32.3±8.9 years and with no evidence of cardiac disease. They underwent cardiac MRI to determine morphological and functional changes of the heart and to detect areas of hyperenhancement after IV administration of gadolinium.Results:At least one abnormality on cardiac MRI was observed in 20/30 patients (66.67%). Myocardial oedema was observed in 3 patients (10.0%) and late gadolinium enhancement in only 1 patient (3.3%). Pericardial effusion was found in 3 patients (10.0 %), global hypokinesia in 6 patients (20.0%) and intra-cardiac thrombosis in only 1 patient (3.3%). Pulmonary artery was dilated in 4 patients (13.3%). Left ventricular and right ventricular end diastolic volume were altered in 4 patients (13.3 %) and 7 patients (23.3%) respectively. Also, left ventricular and right ventricular end systolic volume were abnormal in7 patients (23.3%) and 5 patients (16.7%) respectively. Moreover, there was aortic valve regurge in 2 patients (6.7%), tricuspid valve regurge in 9 patients (30%), and mitral valve regurge in 9 patients (30%).Dilated left main coronary artery in 2 patients (6.7%) and arythmogenic right ventricular dysplasia in only one patient 1 patient (3.3%).Conclusion:Behçet’s disease may cause cardiac abnormalities without clinical manifestations and cardiac MRI may represent a tool for early detection of these subtle abnormalities.References:[1]Geri, G., et al., Spectrum of cardiac lesions in Behçet disease: a series of 52 patients and review of the literature. Medicine, 2012.91(1): p. 25-34.Figure 1.Cardiac MRI in 32 year-old female patient with Behçet’s disease for 3 years.Acknowledgments: :The authors would like to acknowledge Ahmed El Bahy for his assistance with this studyDisclosure of Interests:None declared


2018 ◽  
Vol 121 (8) ◽  
pp. e56-e57
Author(s):  
Yusuf Ziya Şener ◽  
Metin Okşul ◽  
Berkan Armağan ◽  
Alper Sarı ◽  
Ergün Barış Kaya ◽  
...  

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