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Marantic or Non-Bacterial Thrombotic Endocarditis

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Introduction
Marantic endocarditis (MAE), “verrucous” or “Libman Sachs
Endocarditis” are all different synonyms of the nowadays agreed
term non-bacterial thrombotic endocarditis (NBTE), which is
    
infective endocarditis. MAE is associated with an autoimmune-
     
           
     
(SLE), but also in terminal malignancies. The incidence of MAE is
   

      
and management.
Aetiology and Pathophysiology
MAE is most commonly associated with malignancy with

cancer to adenocarcinoma of the lungs. Overall, adenocarcinomas
have been shown to be mostly associated with MAE and of those
    
       
        
       


The trigger for MAE and how it relates to commonly associated
       
  
       
       
      
         

Presentation and Diagnosis
       
       
cerebrovascular events, such as strokes or transient ischemic
attacks [6]. Emboli can ultimately affect any arterial system
        
acute mesenteric ischaemia [3]. Localisation of causation can be
        
      
         
with SLE may describe a history of rashes, arthralgia and renal
      

Valvular vegetations in MAE are usually small, broad based
         
        
       
   


       
      
       
rule autoimmune conditions such as SLE. As with conventional
        

over transthoracic [7] in demonstrating vegetations.
Management

        
studies. This is in stark contrast to infective endocarditis, which has


management of the underlying condition likely causing MAE [9].
     
     
       

ISSN: 2643-6884 DOI: 10.33552/OJCR.2019.01.000519
Online Journal of
Cardiovascular Research
Mini Review Copyright © All rights are reserved by Viren Ahluwalia
Marantic or Non-Bacterial Thrombotic Endocarditis
Viren Ahluwalia*, Walid Safwat and Michael Kuehl
Department of Cardiology, UK
*Corresponding author:      

Received Date: March 11, 2019
Published Date: March 27, 2019
This work is licensed under Creative Commons Attribution 4.0 License

Online Journal of Cardiovascular Research Volume 1-Issue 4
Citation: 
. .
Page 2 of 2
         
       
      
         
anticoagulants like direct thrombin or factor Xa inhibitors have


is common. Therefore, some investigators suggest anticoagulation

[10]. Surgery is not routinely recommended to treat MAE. However,
        

    

         
as it is associated with disseminated and advanced underlying
malignancy.
Conclusion
Figure 1: TOE Features: MAE most commonly affects the left
side of the heart, commonly involving the basal and mid portion
of the valve. Masses traditionally have irregular borders, variable
echo density and an absence of independent motion.
       
         
    
       
         
     

serial blood cultures to rule out infective endocarditis followed by
investigation and treatment of the underlying causative condition
      



          
  

Acknowledgement
None.


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1.           
    
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2.          


3. 
    

  
      

 

6.             
     

7.             
     
  

 


        
  

9.            
    

10.          
        
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... 4 It has been described more often as a complication of antiphospholipid syndrome, systemic lupus erythematosus, and malignancy. 5 Strokes and other embolic complications are the most common presentation of marantic endocarditis. 5 The pathophysiology is not well understood and the management often involves treating the underlying condition and anticoagulation. ...
... 5 Strokes and other embolic complications are the most common presentation of marantic endocarditis. 5 The pathophysiology is not well understood and the management often involves treating the underlying condition and anticoagulation. 5 Cardiac magnetic resonance is a sensitive, non-invasive investigation for myocarditis. ...
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Malignant peritoneal mesothelioma (MPM) is a rare diagnosis that presents with difficulties in diagnosis and management. This article reports a case of an 88-year-old male who presented with a 2-week history of abdominal distention and bloating. He worked at an insulation production factory between the ages of 23 and 25 years with presumed asbestos exposure. On the computed tomography scan of the abdomen/pelvis, the patient was found to have diffuse omental, peritoneal, and mesenteric nodularity with moderate to large ascites. Omental biopsy revealed MPM. The overall prognosis of MPM remains poor, with a median survival time of 12 months at the time of diagnosis. Treatment modalities offered in the United States include chemotherapy alone, cytoreductive surgery alone, or cytoreductive surgery/chemotherapy combination.
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Libman-Sacks endocarditis, characterized by Libman-Sacks vegetations, is common in patients with systemic lupus erythematosus and is commonly complicated with embolic cerebrovascular disease. Thus, accurate detection of Libman-Sacks vegetations may lead to early therapy and prevention of their associated complications. Although two-dimensional (2D) transesophageal echocardiography (TEE) has high diagnostic value for detection of Libman-Sacks vegetations, three-dimensional (3D) TEE may allow improved detection, characterization, and clinical correlations of Libman-Sacks vegetations. Twenty-nine patients with systemic lupus erythematosus (27 women; mean age, 34 ± 12 years) prospectively underwent 40 paired 3D and 2D transesophageal echocardiographic studies and assessment of cerebrovascular disease manifested as acute clinical neurologic syndromes, neurocognitive dysfunction, or focal brain injury on magnetic resonance imaging. Initial and repeat studies in patients were intermixed in a blinded manner with paired studies from healthy controls, deidentified, coded, and independently interpreted by experienced observers unaware of patients' clinical and imaging data. The results of 3D TEE compared with 2D TEE were more often positive for mitral or aortic valve vegetations, and 3D TEE detected more vegetations per study and determined larger sizes of vegetations (P ≤ .03 for all). Also, 3D TEE detected more vegetations on the anterior mitral leaflet, anterolateral and posteromedial scallops, and ventricular side or both atrial and ventricular sides of the leaflets (P < .05 for all). In addition, 3D TEE detected more vegetations on the aortic valve left and noncoronary cusps, coronary cusps' tips and margins, and aortic side or both aortic and ventricular sides of the cusps (P ≤ .01 for all). Furthermore, 3D TEE more often detected associated mitral or aortic valve commissural fusion (P = .002). Finally, 3D TEE detected more vegetations in patients with cerebrovascular disease (P = .01). Three-dimensional TEE provides clinically relevant additive information that complements 2D TEE for the detection, characterization, and association with cerebrovascular disease of Libman-Sacks endocarditis. Published by Elsevier Inc.
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The aim of this study was to determine whether Libman-Sacks endocarditis is a pathogenic factor for cerebrovascular disease (CVD) in systemic lupus erythematosus (SLE). A cardioembolic pathogenesis of SLE CVD manifested as: 1) neuropsychiatric systemic lupus erythematosus (NPSLE), including stroke and transient ischemic attacks (TIA); 2) neurocognitive dysfunction; and 3) magnetic resonance imaging of focal brain lesions has not been established. A 6-year study of 30 patients with acute NPSLE (27 women, 38 ± 12 years of age), 46 age- and sex-matched SLE controls without NPSLE (42 women, 36 ± 12 years of age), and 26 age- and sex-matched healthy controls (22 women, 34 ± 11 years of age) who underwent clinical and laboratory evaluations, transesophageal echocardiography, carotid duplex ultrasound, transcranial Doppler ultrasound, neurocognitive testing, and brain magnetic resonance imaging/magnetic resonance angiography. Patients with NPSLE were re-evaluated after 4.5 months of therapy. All patients were followed clinically for a median of 52 months. Libman-Sacks vegetations (87%), cerebromicroembolism (27% with 2.5 times more events per hour), neurocognitive dysfunction (60%), and cerebral infarcts (47%) were more common in NPSLE than in SLE (28%, 20%, 33%, and 0%) and healthy controls (8%, 0%, 4%, and 0%, respectively) (all p ≤ 0.009). Patients with vegetations had 3 times more cerebromicroemboli per hour, lower cerebral blood flow, more strokes/TIA and overall NPSLE events, neurocognitive dysfunction, cerebral infarcts, and brain lesion load than those without (all p ≤ 0.01). Libman-Sacks vegetations were independent risk factors of NPSLE (odds ratio [OR]: 13.4; p < 0.001), neurocognitive dysfunction (OR: 8.0; p = 0.01), brain lesions (OR: 5.6; p = 0.004), and all 3 outcomes combined (OR: 7.5; p < 0.001). Follow-up re-evaluations in 18 of 23 (78%) surviving patients with NPSLE demonstrated improvement of vegetations, microembolism, brain perfusion, neurocognitive dysfunction, and lesion load (all p ≤ 0.04). Finally, patients with vegetations had reduced event-free survival time to stroke/TIA, cognitive disability, or death (p = 0.007). The presence of Libman-Sacks endocarditis in patients with SLE was associated with a higher risk for embolic CVD. This suggests that Libman-Sacks endocarditis may be a source of cerebral emboli.
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We evaluated the prevalence and progression of Libman-Sacks endocarditis in patients with systemic lupus erythematosus and any association between this valvulopathy and their clinical and laboratory characteristics. Doppler echocardiography was performed in 342 consecutive patients with systemic lupus erythematosus (297 females and 45 males). The clinical and laboratory data were recorded. Patients were reevaluated after a follow-up period of 4 years. Libman-Sacks endocarditis was found in 38 patients (11%). In 24 of 38 patients, mitral valve involvement was found, resulting in regurgitation in all (mild in 18, moderate in 4, and severe in 2), whereas stenosis co-occurred with regurgitation in 9 patients (mild in 6 and moderate in 3). Thirteen (34%) of 38 patients had aortic valve involvement; 11 had regurgitation (mild) and 8 had stenosis (mild), coexistent with regurgitation in 6 of them. One patient had mild tricuspid regurgitation. A significant association was found between Libman-Sacks endocarditis and disease duration and activity, thromboses, stroke, thrombocytopenia, anticardiolipin antibodies, and antiphospholipid syndrome. During the follow-up period, 252 of 342 patients were reevaluated echocardiographically. Among the 38 patients with Libman-Sacks vegetations, 5 with mild mitral regurgitation at the beginning developed moderate (n=4) and severe mitral regurgitation (n=1), 2 patients with mitral stenosis (mild in 1 and moderate in 1) developed severe mitral regurgitation, and 2 patients with mild aortic regurgitation developed moderate and severe mitral regurgitation, whereas a significant deterioration of aortic stenosis was found. Two patients who were candidates for surgery died. Among the 213 patients without vegetations at the beginning, 8 developed new Libman-Sacks lesions. Libman-Sacks vegetations can be found in approximately 1 of 10 patients with systemic lupus erythematosus, and they are associated with lupus duration, disease activity, anticardiolipin antibodies, and antiphospholipid syndrome manifestations. A progression of valve lesions may occur during long-term follow-up.
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