Antiphospholipid antibody syndrome

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

This chapter reviews antiphospholipid antibody syndrome–its features, diagnosis, and therapy. Manifestations of APLA including stroke, venous thrombosis, thrombocytopenia, and pregnancy complications are discussed. APLA are antibodies directed against certain phospholipids. They are found in a variety of clinical situations. APLA are important to detect because in certain patients they are associated with a syndrome which includes a hypercoagulable state, thrombocytopenia, fetal loss, dementia, strokes, optic changes, Addisonõs disease, and skin rashes. The underlying mechanism leading to the clinical syndrome associated with APLA is still unknown. Perhaps the antibodies inhibit the function of proteins C or S, damage the endothelium, activate platelets, or inhibit prostacyclin. Despite several decades of research, the etiology of the thrombotic tendency associated with APLA remains unknown.

Original languageEnglish (US)
Title of host publicationHemostasis and Thrombosis, Third Edition
PublisherSpringer International Publishing
Pages95-99
Number of pages5
ISBN (Electronic)9783319093123
ISBN (Print)9783319093116
DOIs
StatePublished - Jan 1 2015

ASJC Scopus subject areas

  • General Medicine

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