scholarly journals Primary Antiphospholipid Syndrome Presenting as Bell Palsy without Cerebral Arterial Thrombosis

2017 ◽  
Vol 92 (2) ◽  
pp. 219-223
Author(s):  
Bo Young Kim ◽  
Jon Woon Chae ◽  
Hyun-Sook Kim
Lupus ◽  
2007 ◽  
Vol 16 (10) ◽  
pp. 782-787 ◽  
Author(s):  
A.W.S. de Souza ◽  
N.P. Silva ◽  
J.F. de Carvalho ◽  
V. D'Almeida ◽  
M.A.E. Noguti ◽  
...  

2012 ◽  
Vol 25 (1) ◽  
pp. 275-280 ◽  
Author(s):  
E.M. Zardi ◽  
D.M. Zardi ◽  
Z. Lazarevic ◽  
S. Santucci ◽  
F. D'Errico ◽  
...  

We describe the case of a 45-year-old woman who had drawn our attention for some recent episodes of transient global amnesia that, upon further examination, resulted from ischemic events caused by multiple arterial thrombosis (bilateral internal carotid occlusion, significant stenosis of the right external carotid, mild stenosis of the right vertebral artery, right anterior cerebral artery occlusion and severe stenosis of the anterior descending coronary artery) due to primary antiphospholipid syndrome. Revascularisation of either carotid was not attempted. A percutaneous intervention in the anterior descending coronary artery stenosis was performed successfully. Due to severe arterial thrombosis, the patient was discharged with only duplex antiplatelet treatment and subcutaneous anticoagulant therapy, since immunotherapy is not indicated in primary APS. The occurrence of transient global amnesia should raise the suspicion of APS.


Author(s):  
Jozélio Freire de Carvalho ◽  
Maria Betania Pereira Toralles ◽  
Maria Isabel Figueiredo Sousa ◽  
Thelma Larocca Skare

2021 ◽  
pp. 1-4
Author(s):  
Ram Gelman ◽  
Fadi Kharouf ◽  
Yuval Ishay ◽  
Alexander Gural

Antiphospholipid syndrome and cold agglutinin-mediated autoimmune hemolytic anemia are 2 distinct immune-mediated hematologic disorders. While no clear association exists between these 2 entities, complement activation is known to occur in both of them. Herein, we report a unique case of cold agglutinin hemolytic anemia in a patient with a known primary antiphospholipid syndrome.


2020 ◽  
Vol 2020 (12) ◽  
Author(s):  
Stathis Tsiakas ◽  
Chrysanthi Skalioti ◽  
Paraskevi Kotsi ◽  
Ioannis Boletis ◽  
Smaragdi Marinaki

ABSTRACT Antiphospholipid syndrome (APS) is a systemic autoimmune disease defined by the presence of antiphospholipid antibodies in association with thrombotic events and/or obstetric complications. Renal involvement is not infrequent in both primary and secondary APS. Kidney manifestations comprise a wide range of clinical features, including hypertension, major renal vessel thrombosis or microvascular endothelial injury, also described as APS nephropathy. In the absence of a thrombotic event, clinical manifestations of APS are often non-specific. We recently encountered a case of primary APS in a young male with newly diagnosed hypertension and renal impairment. The diagnosis of APS was initially suspected by his kidney biopsy findings, when electron microscopy examination showed the features of chronic microangiopathy, and was later confirmed by a triple positive antiphospholipid antibody profile and multiple organ involvement.


2011 ◽  
Vol 9 (S1) ◽  
Author(s):  
E Merlin ◽  
E Doré ◽  
S Chabrier ◽  
A Marques Verdier ◽  
JL Stéphan

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