A case of Limited Scleroderma Associated with Antiphospholipid Syndrome / 대한류마티스학회지
The Journal of the Korean Rheumatism Association
;
: 103-107, 1998.
Artículo
en Coreano
| WPRIM
| ID: wpr-184303
ABSTRACT
The antiphospholipid syndrome is characterized by arterial thrombosis, venous thrombosis, pregnancy wastage, and thrombocytopenia associated with a persis tently positive lupus anticoagulant and/or moderate to high positive anticardiolipin antibodies(IgG or IgM). The antiphospholipid antibodies have been detected in many medical conditions, but the antiphospholipid syndrome (APS) has mainly been restricted to the primary antiphospholipid syndrome and APS associated with systemic lupus erythematosus. Rarely, the APS has been reported in other autoimmune disorders in the literature. We describe a woman with a limited form of scleroderma and the APS manifested by complete occlusion of left axillary artery with probable thrombotic occlusive nature, thrombocytope nia, prolonged aPTT, and persistently positive lupus anticoagulant.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Arteria Axilar
/
Trombocitopenia
/
Trombosis
/
Inhibidor de Coagulación del Lupus
/
Síndrome Antifosfolípido
/
Anticuerpos Antifosfolípidos
/
Trombosis de la Vena
/
Esclerodermia Limitada
/
Lupus Eritematoso Sistémico
Límite:
Femenino
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
The Journal of the Korean Rheumatism Association
Año:
1998
Tipo del documento:
Artículo
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