Acquired pure red cell aplasia in a child.
J Postgrad Med
;
2002 Jan-Mar; 48(1): 37-8
Artículo
en Inglés
| IMSEAR
| ID: sea-117186
ABSTRACT
Primary acquired pure red cell aplasia is a rare occurrence in childhood. An eleven-year old boy presented to us with pallor, which required multiple packed red cell transfusions. He did not have hepatosplenomegaly, jaundice or lymphadenopathy. Bone marrow examination revealed the diagnosis of pure red cell aplasia. All possible investigations were done to exclude secondary causes of pure red cell aplasia. No secondary cause was found on investigations. Rheumatoid factor and anti-nuclear antibodies were positive. He was started on oral steroids, to which he did not respond. He was then given cyclosporine A. Response to cyclosporine was dramatic and the child now does not require any transfusions.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Transfusión Sanguínea
/
Médula Ósea
/
Humanos
/
Masculino
/
Hemoglobinas
/
Niño
/
Enfermedad Crónica
/
Ciclosporina
/
Aplasia Pura de Células Rojas
/
Inmunosupresores
Idioma:
Inglés
Revista:
J Postgrad Med
Año:
2002
Tipo del documento:
Artículo
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