scholarly journals A male patient with myocardial infarction as a first manifestation of antiphospholipid syndrome — treatment with rivaroxaban

2016 ◽  
pp. 19-22 ◽  
Author(s):  
Agata Bryk ◽  
Anetta Undas
Angiology ◽  
2001 ◽  
Vol 52 (11) ◽  
pp. 785-788 ◽  
Author(s):  
Bruno Laganà ◽  
Luigi Baratta ◽  
Luigi Tubani ◽  
Vincenzina Golluscio ◽  
Massimo Delfino ◽  
...  

2021 ◽  
Author(s):  
R Plöger ◽  
P Kosian ◽  
D Momcilovic ◽  
J Luetkens ◽  
U Gembruch ◽  
...  

2015 ◽  
Vol 3 (4) ◽  
pp. 705-709 ◽  
Author(s):  
Marija Vavlukis ◽  
Irina Kotlar ◽  
Emilija Chaparoska ◽  
Bekim Pocesta ◽  
Hristo Pejkov ◽  
...  

AIM: We are presenting an uncommon case of pulmonary embolism, followed with an acute myocardial infarction, in a patient with progressive systemic sclerosis.CASE PRESENTATION: A female 40 years of age was admitted with signs of pulmonary embolism, confirmed with CT scan, which also reviled a thrombus in the right ventricle. The patient had medical history of systemic sclerosis since the age of 16 years. She suffered an ischemic stroke 6 years ago, but she was not taking any anticoagulant or antithrombotic medications ever since. She received a treatment with thrombolytic therapy, and subsequent UFH, but, on the second day after receiving fibrinolysis, she felt chest pain accompanied with ECG changes consistent for ST-segment elevation myocardial infarction (STEMI). Urgent coronary angiography was undertaken, which reviled cloths causing total occlusion in 4 blood vessels, followed with thromboaspiration, but without successful reperfusion. Several hours later the patient developed rapid deterioration with letal ending. During the very short hospital course, blood sampling reviled presence of antiphospholipid antibodies.CONCLUSION: The acquired antiphospholipid syndrome is common condition in patients with systemic autoimmune diseases, but relatively rare in patients with systemic sclerosis. Never the less, we have to be aware of it when treating the patients with systemic sclerosis.


2007 ◽  
Vol 83 (3) ◽  
pp. 1170-1171 ◽  
Author(s):  
Ibrahim S. Abu Romeh ◽  
Adnan K. Chhatriwalla ◽  
Fernando A. Atik ◽  
Deepak L. Bhatt ◽  
Jose L. Navia

Author(s):  
Karolina Semczuk-Kaczmarek ◽  
Anna E. Platek ◽  
Anna Ryś-Czaporowska ◽  
Filip M. Szymanski ◽  
Krzysztof J. Filipiak

2016 ◽  
Vol 4 (1) ◽  
pp. 15
Author(s):  
Xiao-yan Chen ◽  
Fan-liang Kong ◽  
Tong-guo Wu

Type A aortic dissection is a catastrophic clinical entity involving the ascending aorta. In this case report, a patient was admitted to the emergency room with a presentation resembling acute myocardial infarction (AMI) that led to the inappropriate administration of anticoagulant agents or platelet. This is a case report of a 69-year-old male patient with early misdiagnosis and analysis of type A aortic dissection with discussion on the causes of misdiagnosis in light of the literature.


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