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A Case of Acquired Glanzmann's Thrombasthenia
Korean Journal of Hematology ; : 183-187, 2005.
Artículo en Coreano | WPRIM | ID: wpr-720487
ABSTRACT
Glanzmann's thrombasthenia (GT) is a rare inherited platelet disorder, which is characterized by a complete lack of platelet aggregation due to a deficiency or abnormality of the membrane glycoprotein IIb/IIIa complex. Anti-GPIIb/IIIa antibodies have also been identified to cause platelet dysfunction in patients with a normal platelet count, but this has only been rarely encountered. The condition is also known as acquired GT. Herein, we describe a patient with acquired GT and a history of Evans' syndrome, who presented with severe bleeding and platelet dysfunction, but with a normal platelet count and GP IIb/IIIa expression.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Recuento de Plaquetas / Plaquetas / Trombastenia / Glicoproteínas de Membrana / Agregación Plaquetaria / Hemorragia / Anticuerpos Tipo de estudio: Estudio pronóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Hematology Año: 2005 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Recuento de Plaquetas / Plaquetas / Trombastenia / Glicoproteínas de Membrana / Agregación Plaquetaria / Hemorragia / Anticuerpos Tipo de estudio: Estudio pronóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Hematology Año: 2005 Tipo del documento: Artículo