• Department of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P. R. China;
WUYu, Email: wu_yu@scu.edu.cn
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Objective To analyze the clinical and immunological characteristics of 26 patients with antiphospholipid syndrome (APS). Methods The clinical and immunological features of APS in 26 patients treated between January 2009 and January 2012 were analyzed retrospectively. Results The study consisted of 8 male and 18 female patients with a mean age of 38 years at diagnosis. Seven patients had primary APS. Nineteen patients had APS associated with autoimmune diseases, including 11 cases of systemic lupus erythematosus. Seventy-five percent of the patients had thrombosis, 16 had venous thrombosis, 7 had arterial thrombosis, and 2 had both arterial and venous thrombosis. The deep veins of the lower limbs and the cerebral arterial circulation were the most common sites of venous and arterial thrombosis. Fetal morbidity rate of 16 married women in our study was 43.8%. Thrombocytopenia and anemia were present in 57.7% and 69.2% of the patients respectively. Conclusion APS is characterized by recurrent thrombosis, pregnancy morbidity and positive antiphospholipid antibodies tests. Early diagnosis and management is essential for APS.

Citation: CHENXin-yi, SUNRui-xue, WUYu. Clinical and Immunological Characteristics of Antiphospholipid Syndrome. West China Medical Journal, 2014, 29(4): 612-615. doi: 10.7507/1002-0179.20140185 Copy

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