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.
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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