Antiphospholipid Syndrome-induced Ischemic Stroke Following Pembrolizumab: case report and systematic review

Lung Cancer ◽  
2021 ◽  
Author(s):  
Vito Tota ◽  
Marie Dagonnier ◽  
Didier Wery ◽  
Laure Binet ◽  
Nathalie Nagy ◽  
...  
2020 ◽  
Vol 47 (5) ◽  
pp. 386-392 ◽  
Author(s):  
Alessandro Sgreccia ◽  
Giuseppe Carità ◽  
Oguzhan Coskun ◽  
Federico Di Maria ◽  
Hakim Benamer ◽  
...  

Lupus ◽  
2020 ◽  
Vol 29 (6) ◽  
pp. 631-639 ◽  
Author(s):  
Marta Skoczynska ◽  
Mark A Crowther ◽  
Malgorzata Chowaniec ◽  
Monika Ponikowska ◽  
Shruti Chaturvedi ◽  
...  

Objective The purpose of this study was to characterize the role of eculizumab, a monoclonal antibody against the terminal complement component C5, in patients with catastrophic antiphospholipid syndrome (CAPS). Methods We present a case report of a patient with systemic lupus erythematosus (SLE) and CAPS treated with eculizumab, as well as results of a systematic review of the literature. Results Including our patient, we identified 11 case reports of patients with CAPS treated with eculizumab. All of them had partial or total remission of symptoms. Conclusion Data on eculizumab efficacy in CAPS are promising but are limited to single case reports. More studies are needed to develop evidence-based recommendations for eculizumab use in CAPS.


Author(s):  
Christian Basile ◽  
Costantino Mancusi ◽  
Paola Gargiulo ◽  
Pasquale Perrone Filardi ◽  
Cinzia Perrino ◽  
...  

Ischemic stroke represents one of the most important health problems in industrialized countries, both for epidemiological and socio-economic impact. The presence of thrombi in the aorta is rare and its treatment has not been uniquely defined. Here we report the case of an 82-years-old man with aortic thrombosis and acute ischemic stroke.


2019 ◽  
Vol 19 (3) ◽  
pp. 281-288 ◽  
Author(s):  
Maria Giulia Tinti ◽  
Vincenzo Carnevale ◽  
Michele Inglese ◽  
Francesca Molinaro ◽  
Marco Bernal ◽  
...  

2020 ◽  
Vol 8 ◽  
Author(s):  
Teresa Giani ◽  
Angela Mauro ◽  
Giovanna Ferrara ◽  
Rolando Cimaz

Antiphospholipid syndrome (APS) is a rare condition in childhood, but even more in the neonatal age. Most neonatal cases are considered a passively acquired autoimmune disease, due to a transplacental passage of maternal antiphospholipid antibodies (aPL) from mothers with primary or secondary APS or, more often, from asymptomatic aPL carriers. Exceedingly unusual is the neonatal de novo production of aPL. We present four infants with presumed perinatal stroke in presence of increased and persistent aPL levels, even after 6 months of life, opening the window on a gray zone related to the origin of these antibodies (maternal or neonatal) and on their role in the pathogenesis of stroke.


2006 ◽  
Vol 26 (10) ◽  
pp. 1518-1525 ◽  
Author(s):  
Shawnna L Patterson ◽  
Marian P LaMonte ◽  
Jamal A Mikdashi ◽  
Stuart T Haines ◽  
Marcie J Hursting

VASA ◽  
2020 ◽  
pp. 1-6 ◽  
Author(s):  
Marina Di Pilla ◽  
Stefano Barco ◽  
Clara Sacco ◽  
Giovanni Barosi ◽  
Corrado Lodigiani

Summary: A 49-year-old man was diagnosed with pre-fibrotic myelofibrosis after acute left lower-limb ischemia requiring amputation and portal vein thrombosis. After surgery he developed heparin-induced thrombocytopenia (HIT) with venous thromboembolism, successfully treated with argatroban followed by dabigatran. Our systematic review of the literature supports the use of dabigatran for suspected HIT.


2019 ◽  
Author(s):  
De Marchi Lucrezia ◽  
M K de Filette Jeroen ◽  
Sol Bastiaan ◽  
E Andreescu Corina ◽  
Kunda Rastislav ◽  
...  

2012 ◽  
Vol 3 (5) ◽  
pp. 455-457
Author(s):  
Dr .KOUSHIK GUDAVALLI ◽  
◽  
Dr .SHILPA CHIKATI ◽  
Dr .MOHAN RAO JAKKAMPUTI ◽  
Dr .KAMAL LOCHAN BEHERA ◽  
...  

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