Lupus anticoagulant (LA) is made up of heterogeneous IgG and IgM antibodies
that prolong clotting times in vitro and is associated with an increased r
ate of both thrombosis and hemorrhage in vivo, although thrombosis is far m
ore common. Many mechanisms of action have been explored, but none explains
the coagulation abnormality of every sample tested. Binding of these antib
odies to protein phospholipid complexes provides a unifying model. Antiphos
pholipid antibodies (APAs) are found in adult patients with a variety of di
sorders or as an isolated finding. The association of LA and anticardiolipi
n antibodies (ACAs) with thrombosis in adults has been established, althoug
h there is no test as yet to predict thrombotic risk for an asymptomatic af
fected individual. The presentation of thrombosis with postinfectious APA i
s uncommon in adults.
Children who present with thrombosis and LA are found to have underlying di
sorders similar to those of adults. Although the presentation of thrombosis
in children with postinfectious LA is rare, the association is established
. LA-positive children with thrombosis have manifested a severe acquired de
ficiency of protein S; LA-positive children with hemorrhage have manifested
an acquired deficiency of prothrombin, The association of thrombosis with
ACA-positive children has been reported. Further work to determine the epid
emiology, mechanism of action, and thrombotic potential of APA in children
is warranted to better understand, prevent, and treat thrombotic and hemorr
hagic complications.