Background: The antiphospholipid syndrome is an autoimmune, prothrombotic and systemic disorder characterized by arterial and/or venous thrombosis, recurrent fetal loss and persistently elevated antiphospholipid antibody titers.

Aims: To identify the various forms of manifestation of antiphospholipid syndrome

Methods: A retrospective, longitudinal and descriptive study in which the cases of arterial and venous thrombosis associated with thrombophilia

type antiphospholipid syndrome presented during the period from 2016 to 2018 in a Hospital of Veracruz, Mexico were analyzed.

Results: We found 7 patients with venous and arterial thrombotic symptoms that were studied antiphospholipid syndrome, the most affected gender was the female and the predominant age group was 21-30 years. The thrombotic event with the highest incidence was in the deep venous system of the pelvic extremities in 5 patients, in one case it was observed as a complication associated with pulmonary thromboembolism and in another case acute cerebral infarction. The antiphospholipid syndrome was primary in 6 cases and one associated with systemic lupus erythematosus

Conclusion(s): The clinical spectrum of antiphospholipid syndrome is diverse and must be taken into account in order to establish an effective diagnosis and treatment.

Table

Diverse cases of SAF

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ISTH Congress Abstracts - https://abstracts.isth.org/abstract/clinical-spectrum-of-antiphospholipid-syndrome-in-a-second-level-general-hospital/