scholarly journals Nonbacterial thrombotic endocarditis in a patient with primary antiphospholipid syndrome

2018 ◽  
Vol 2018 (6) ◽  
Author(s):  
Natee Sirinvaravong ◽  
Mary C Rodriguez Ziccardi ◽  
Soumya Patnaik ◽  
Mahek Shah ◽  
Gustavo Fernandez ◽  
...  
Keyword(s):  
Antiphospholipid Syndrome ◽  
Primary Antiphospholipid Syndrome ◽  
Nonbacterial Thrombotic Endocarditis

scholarly journals Unusual Case of Nonbacterial Thrombotic Endocarditis Attributable to Primary Antiphospholipid Syndrome

Circulation ◽  
2010 ◽  
Vol 122 (12) ◽  
Author(s):  
Karyne L. Vinales ◽  
Radha S. Gopalan ◽  
Louis A. Lanza ◽  
Steven J. Lester ◽  
Hari P. Chaliki
Keyword(s):  
Antiphospholipid Syndrome ◽  
Unusual Case ◽  
Primary Antiphospholipid Syndrome ◽  
Nonbacterial Thrombotic Endocarditis

Preeclampsia in primary antiphospholipid syndrome is associated with fetal losses and limb ischemia

2021 ◽  
Author(s):  
Jozélio Freire de Carvalho ◽  
Maria Betania Pereira Toralles ◽  
Maria Isabel Figueiredo Sousa ◽  
Thelma Larocca Skare
Keyword(s):  
Antiphospholipid Syndrome ◽  
Limb Ischemia ◽  
Primary Antiphospholipid Syndrome

scholarly journals Cold Agglutinin-Mediated Autoimmune Hemolytic Anemia in Association with Antiphospholipid Syndrome

2021 ◽  
pp. 1-4
Author(s):  
Ram Gelman ◽  
Fadi Kharouf ◽  
Yuval Ishay ◽  
Alexander Gural
Keyword(s):  
Hemolytic Anemia ◽  
Antiphospholipid Syndrome ◽  
Complement Activation ◽  
Autoimmune Hemolytic Anemia ◽  
Cold Agglutinin ◽  
Primary Antiphospholipid Syndrome ◽  
Unique Case ◽  
Hematologic Disorders ◽  
Clear Association ◽  
Immune Mediated

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.

scholarly journals Case of an unusual diagnosis of primary antiphospholipid syndrome with multiple clinical complications

2020 ◽  
Vol 2020 (12) ◽  
Author(s):  
Stathis Tsiakas ◽  
Chrysanthi Skalioti ◽  
Paraskevi Kotsi ◽  
Ioannis Boletis ◽  
Smaragdi Marinaki
Keyword(s):  
Antiphospholipid Syndrome ◽  
Thrombotic Event ◽  
Renal Involvement ◽  
Clinical Manifestations ◽  
Young Male ◽  
Multiple Organ ◽  
Systemic Autoimmune Disease ◽  
Antiphospholipid Antibody ◽  
Primary Antiphospholipid Syndrome ◽  
Wide Range

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.

scholarly journals Infantile de novo primary antiphospholipid syndrome revealed by neonatal stroke

2011 ◽  
Vol 9 (S1) ◽  
Author(s):  
E Merlin ◽  
E Doré ◽  
S Chabrier ◽  
A Marques Verdier ◽  
JL Stéphan
Keyword(s):  
Antiphospholipid Syndrome ◽  
De Novo ◽  
Primary Antiphospholipid Syndrome ◽  
Neonatal Stroke
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