Sneddon Syndrome with or without Antiphospholipid Antibodies: A Comparative Study in 46 Patients

Medicine ◽  
1999 ◽  
Vol 78 (4) ◽  
pp. 209-219 ◽  
Author(s):  
Camille Francès ◽  
Thomas Papo ◽  
Bertrand Wechsler ◽  
Jean-Luc Laporte ◽  
Valérie Biousse ◽  
...  
2018 ◽  
Vol 151 (6) ◽  
pp. 215-222 ◽  
Author(s):  
Jaume Alijotas-Reig ◽  
Enrique Esteve-Valverde ◽  
Raquel Ferrer-Oliveras ◽  
Elisa LLurba ◽  
Amelia Ruffatti ◽  
...  

2015 ◽  
Vol 77 (5) ◽  
pp. 817-829 ◽  
Author(s):  
Laure Bottin ◽  
Camille Francès ◽  
Dominique de Zuttere ◽  
Pierre-Yves Boëlle ◽  
Ioan-Paul Muresan ◽  
...  

2021 ◽  
Vol 5 (6) ◽  
Author(s):  
Soukaina Scadi ◽  
Olivier Huttin ◽  
Christine Selton Suty ◽  
Denis Wahl

Abstract Background Cardiac involvement in Sneddon syndrome (SS) is rare, the physiopathology is still unclear. We report a first case of SS without antiphospholipid antibodies who had coexisting ischaemia with no obstructive coronary arteries and aortic valve diseases. Case summary A 34-year-old woman with SS without antiphospholipid antibodies, was admitted for aphasia, and paresthaesia with confirmed right opercular ischaemic lesions at brain magnetic resonance imaging. Transthoracic echocardiographic examination showed akinesis of apical segments, moderate aortic valve stenosis, and moderate aortic insufficiency. Coronary angiogram was normal. Cardiac magnetic resonance showed transmural necrosis in the territory of the left anterior descending artery. Seven years later, our patient had no change or progression of myocardial ischaemic lesions or valvular disease. Conclusion We will discuss different hypothesis, diagnosis, treatment, and evolution of cardiac involvement in SS. Close follow-up should be regularly performed for early diagnosis, hence the importance of multimodality imaging, to guide treatment and prevent further complications.


Neurology ◽  
2012 ◽  
Vol 78 (Meeting Abstracts 1) ◽  
pp. S43.005-S43.005 ◽  
Author(s):  
L. Bottin ◽  
C. Frances ◽  
D. De Zuttere ◽  
P.-Y. Boelle ◽  
I.-P. Muresan ◽  
...  

2018 ◽  
Vol 151 (6) ◽  
pp. 215-222 ◽  
Author(s):  
Jaume Alijotas-Reig ◽  
Enrique Esteve-Valverde ◽  
Raquel Ferrer-Oliveras ◽  
Elisa LLurba ◽  
Amelia Ruffatti ◽  
...  

2020 ◽  
Vol 1 (1) ◽  
pp. 14-15
Author(s):  
Elharrouni A ◽  
Douhi Z ◽  
Achhboune K ◽  
Baybay H ◽  
Elloudi S ◽  
...  

We report a 40-year-old female. The high blood pressure was found in Family history, hospitalized in neurology for recurrent ischemic stroke so the etiological assessment was negative, opinion was sought for lesions of livedo at the level of the members back to 2 years without the concept of miscarriage or Raynaud’s phenomenon, neither photosensitivity nor a dry syndrome. Dermatologic examination showed dusky erythematous to violaceous, irregular, broken circular segments, resulting in a seemingly larger pattern, located on limbs, trunk, and buttocks, exaggerated by the cold and persistent on warming. A report looking for the antiphospholipid antibodies syndrome was positive and the skin biopsy was in favor of a Sneddon syndrome. The patient was treated by anticoagulants and antiplatelet agents with good evolution.


2020 ◽  
Vol 14 (2) ◽  
Author(s):  
Ziani J ◽  
Douhi Z ◽  
Bennani M ◽  
Elloudi S ◽  
Baybay H ◽  
...  

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